Other products from "GRAMEDICA"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M621OW30LBS18MM0 GM-500-18 OW3.0LBS-18MM osteo-WEDGE 3.0mm x 18mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 18mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 18mm Locking Bone Screw
2 M621OW30LBS16MM0 GM-500-16 OW3.0LBS-16MM osteo-WEDGE 3.0mm x 16mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 16mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 16mm Locking Bone Screw
3 M621OW30LBS10MM0 GM-500-10 OW3.0LBS-10MM osteo-WEDGE 3.0mm x 10mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 10mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 10mm Locking Bone Screw
4 M621OW25LBS10MM0 GM-200-10 OW2.5LBS-10MM osteo-WEDGE 2.5mm x 10mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 10mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 2.5mm x 10mm Locking Bone Screw
5 M621OTSS0 OT-SS OT-SS The opti-Toe Small Straight Implant is comprised of two mated components (proxim The opti-Toe Small Straight Implant is comprised of two mated components (proximal and middle phalangeal) which join together to form a single intramedullary fixation unit. Indications: The GraMedica opti-Toe Device is indicate for reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. The GraMedica opti-Toe components are to be cemented in place and assembled for reconstruction of the toe. Patients should protect weight-bearing or heal bearing until healing has occurred. HTY Pin, Fixation, Smooth 2 opti-Toe Small Straight
6 M621OTSA0 OT-SA OT-SA The Opti-Toe-Small Angle Implant is comprised of two mated components (proximal The Opti-Toe-Small Angle Implant is comprised of two mated components (proximal and middle phalangeal) which join together to form a single intramedullary fixation unit. Indications: The GraMedica opti-Toe Device is indicate for reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. The GraMedica opti-Toe components are to be cemented in place and assembled for reconstruction of the toe. Patients should protect weight-bearing or heal bearing until healing has occurred. HTY Pin, Fixation, Smooth 2 Opti-Toe-Small Angle
7 M621HYPII070 HYP II-07 HYP II-07 HyProCure II Sinus Tarsi Implant Size 07. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 07. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Sinus Tarsi Stent Size 07
8 M621HYPII060 HYP II-06 HYP II-06 HyProCure II Sinus Tarsi Implant Size 06. Indications: HyProCure II (HYP II an HyProCure II Sinus Tarsi Implant Size 06. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Sinus Tarsi Stent Size 06
9 M621GM504090 GM-504-09 GM-504-09 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 9 Degree Angulated Bone Plate Implant, Large
10 M621OW25LBS22MM0 GM-200-22 OW2.5LBS-22MM osteo-WEDGE 2.5mm x 22mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 22mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 2.5mm x 22mm Locking Bone Screw
11 M621OW25LBS20MM0 GM-200-20 OW2.5LBS-20MM osteo-WEDGE 2.5mm x 20mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 20mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC Screw, Fixation, Bone 2 osteo-WEDGE 2.5mm x 20mm Locking Bone Screw
12 M621OW25LBS14MM0 GM-200-14 OW2.5LBS-14MM osteo-WEDGE 2.5mm x 14mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 14mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 2.5mm x 14mm Locking Bone Screw
13 M621HYPSTDS0 11-363-11 11cm/4.5" HYP-ST-DS Reusable HyProCure SinusTarsi Decompression Scissors for dissecting and cutting Reusable HyProCure SinusTarsi Decompression Scissors for dissecting and cutting soft tissue. HRR Scissors, Orthopedic, Surgical 1 HYP Sinus Tarsi Decompression Scissors
14 M621HYPII50 HYP II-5 HYP II-5 HyProCure II Driver instrument. For use with the HyProCure II Sinus Tarsi Impla HyProCure II Driver instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Driver
15 M621HYPGUIDEWIRES0 HYP-GuideWires HYP-GuideWires Guide Wire, a reusable instrument, for use with the HyProCure or HyProCure II Si Guide Wire, a reusable instrument, for use with the HyProCure or HyProCure II Sinus Tarsi Implant System. Indications: HyProCure is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 Guide Wire
16 M621HYP100 HYP-10 HYP-10 HyProCure Sinus Tarsi Implant Size 10. Indications: HyProCure is a talotarsa HyProCure Sinus Tarsi Implant Size 10. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure Size 10
17 M621HYP080 HYP-08 HYP-08 HyProCure Sinus Tarsi Implant Size 08. Indications: HyProCure is a talotarsa HyProCure Sinus Tarsi Implant Size 08. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure Size 08
18 M621GM504180 GM-504-18 GM-504-18 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 18 Degree Angulated Bone Plate Implant, Large
19 M621GM503210 GM-503-21 GM-503-21 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 21 Degree Angulated Bone Plate Implant, Small
20 M621GM503120 GM-503-12 GM-503-12 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 12 Degree Angulated Bone Plate Implant, Small
21 M621GM503090 GM-503-09 GM-503-09 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 9 Degree Angulated Bone Plate Implant, Small
22 M621GM150010 GM-150-01 GM-150-01 osteo-WEDGE Depth Gauge Sleeve, a reusable instrument, for use with the osteo-WE osteo-WEDGE Depth Gauge Sleeve, a reusable instrument, for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE Depth Gauge Sleeve
23 M621CP1510FG0 CP15-10-FG CP15-10-FG HyProCure Sizer 10. Reusable instrument, for use with the HyProCure Sinus Tar HyProCure Sizer 10. Reusable instrument, for use with the HyProCure Sinus Tarsi Implant System. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure Sizer 10
24 M621CARRYINGCASE20 CarryingCase2 CarryingCase2 osteo-WEDGE2 Opening Wedge Bone Locking System -Kit (containing non-sterile sing osteo-WEDGE2 Opening Wedge Bone Locking System -Kit (containing non-sterile single use implants (2.5mm locking bone screws, 3.0mm locking bone screws and bone plates), non-sterile single use temporary tacks and non-sterile reusable instruments). The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE2 Open Wedge Bone Locking System
25 M621OW30LBS26MM0 GM-500-26 OW3.0LBS-26MM osteo-WEDGE 3.0mm x 26mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 26mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 26mm Locking Bone Screw
26 M621OW30LBS14MM0 GM-500-14 OW3.0LBS-14MM osteo-WEDGE 3.0mm x 14mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 14mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 14mm Locking Bone Screw
27 M621HYPIITS120 HYP II-TS-12 HYP II-TS-12 HyProCure II Trial Sizer 12 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 12 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Trial Sizer 12
28 M621HYPIIINSTRAY0 HYPII-INS-TRAY HYPII-INS-TRAY HyProCure II (reusable) Instrument Tray-Kit. The Instrument kit contains seven HyProCure II (reusable) Instrument Tray-Kit. The Instrument kit contains seven Trial Sizers (06mm thru 12mm) one Driver, one Positioning Sleeve and three Guide Wires). For use with the HyProCure II Sinus Tarsi Implants. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion HWC Screw, Fixation, Bone 2 HyProCure II Instrument Tray-Set
29 M621GM503030 GM-503-03 GM-503-03 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 3 Degree Angulated Bone Plate Implant, Small
30 M621GM501040 GM-501-04 GM-501-04 osteo-WEDGE Bone Plate 04mm. Non-sterile single use implant for use with the os osteo-WEDGE Bone Plate 04mm. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE Bone Plate 04mm
31 M621GM501000 GM-501-00 GM-501-00 osteo-WEDGE Bone Plate 00mm. Non-sterile single use implant for use with the os osteo-WEDGE Bone Plate 00mm. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE Bone Plate 00mm
32 M621CP1505FG0 CP15-05-FG CP15-05-FG HyProCure Sizer 05. Reusable instrument, for use with the HyProCure Sinus Tarsi HyProCure Sizer 05. Reusable instrument, for use with the HyProCure Sinus Tarsi Implant System. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure Sizer 05
33 M621CARRYINGCASE0 OWCarryingCase-Kit CarryingCase osteo-WEDGE Opening Wedge Bone Locking System -Kit (containing non-sterile singl osteo-WEDGE Opening Wedge Bone Locking System -Kit (containing non-sterile single use implants (2.5mm locking bone screws, 3.0mm locking bone screws and bone plates), non-sterile single use temporary tacks and non-sterile reusable instruments). The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE Opening Wedge Bone Locking System
34 M621OW30LBS08MM0 GM-500-08 OW3.0LBS-08MM osteo-WEDGE 3.0mm x 08mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 08mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 08mm Locking Bone Screw
35 M621OW25LBS12MM0 GM-200-12 OW2.5LBS-12MM osteo-WEDGE 2.5mm x 12mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 12mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 2.5mm x 12mm Locking Bone Screw
36 M621HYPIITS100 HYP II-TS-10 HYP II-TS-10 HyProCure II Trial Sizer 10 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 10 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Trial Sizer 10
37 M621HYPII110 HYP II-11 HYP II-11 HyProCure II Sinus Tarsi Implant Size 11. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 11. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Sinus Tarsi Stent Size 11
38 M621HYPII100 HYP II-10 HYP II-10 HyProCure II Sinus Tarsi Implant Size 10. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 10. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Sinus Tarsi Stent Size 10
39 M621HYP050 HYP-05 HYP-05 HyProCure Sinus Tarsi Implant Size 05. Indications: HyProCure is a talotarsal HyProCure Sinus Tarsi Implant Size 05. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure Size 05
40 M621GMDSLS0 11-470-11-S (14cm/5.5") GM-DS-LS Reusable Graham Decompression Scissors, straight, for cutting soft tissue. HRR Scissors, Orthopedic, Surgical 1 Graham Decompression Scissors, Straight
41 M621GM504150 GM-504-15 GM-504-15 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 15 Degree Angulated Bone Plate Implant, Large
42 M621GM503060 GM-503-06 GM-503-06 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 6 Degree Angulated Bone Plate Implant, Small
43 M621GM160040 GM-160-04 GM-160-04 osteo-WEDGE2 Drill Guide, a reusable instrument, for use with the osteo-WEDGE O osteo-WEDGE2 Drill Guide, a reusable instrument, for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 Drill Guide
44 M621GM160030 GM-160-03 GM-160-03 osteo-WEDGE2 Drill Guide, a reusable instrument, for use with the osteo-WEDGE O osteo-WEDGE2 Drill Guide, a reusable instrument, for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HRS,HWC Plate, Fixation, Bone,Screw, Fixation, Bone 2 osteo-WEDGE2 Drill Guide
45 M621CP1509FG0 CP15-09-FG CP15-09-FG HyProCure Sizer 09. Reusable instrument, for use with the HyProCure Sinus Tars HyProCure Sizer 09. Reusable instrument, for use with the HyProCure Sinus Tarsi Implant System. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure Sizer 09
46 M621OW30LBS24MM0 GM-500-24 OW3.0LBS-24MM osteo-WEDGE 3.0mm x 24mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 24mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE 3.0mm x 24mm Locking Bone Screw
47 M621OW24TT12MM0 GM-100-12 OW2.4TT-12MM osteo-WEDGE Temporary Tack, 2.4mm x 12mm. Non-sterile single use (disposable) a osteo-WEDGE Temporary Tack, 2.4mm x 12mm. Non-sterile single use (disposable) accessory for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. HWC,HRS Screw, Fixation, Bone,Plate, Fixation, Bone 2 osteo-WEDGE Temporary Tack 2.4mm x 12mm
48 M621HYPIITS110 HYP II-TS-11 HYP II-TS-11 HyProCure II Trial Sizer 11 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 11 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion.. HWC Screw, Fixation, Bone 2 HyProCure II Trial Sizer 11
49 M621HYPIITS080 HYP II-TS-08 HYP II-TS-08 HyProCure II Trial Sizer 08 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 08 instrument. For use with the HyProCure II Sinus Tarsi Implants. The HyProCure II (HYP II and HYP IIs) Sinus Tarsi Implant system is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Trial Sizer 08
50 M621HYPIIPS0 HYPII-PS HYPII-PS HyProCure II Positioning Sleeve instrument. For use with the HyProCure II Sinus HyProCure II Positioning Sleeve instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HWC Screw, Fixation, Bone 2 HyProCure II Positioning Sleeve
Other products with the same Product Code "HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10381780074342 TRUARCHIMP TRUARCHIMP The Integra TruArch subtalar implant is a one-piece titanium implant for treatin The Integra TruArch subtalar implant is a one-piece titanium implant for treating hyperpronation of the foot. It is designed to block forward, downward and medial displacement of the talus, thus allowing normal subtalar joint motion but blocking excessive pronation and the resulting sequela. The implant is offered in 5 sizes ranging from 8mm to 12mm in diameter. The system includes instruments to facilitate the placement of the implants. Integra® TruArch® ASCENSION ORTHOPEDICS, INC.
2 10381780074335 TI6SOLIDIMP TI6SOLIDIMP The Integra Ti6 Internal Fixation System is comprised of Solid Bone screws use The Integra Ti6 Internal Fixation System is comprised of Solid Bone screws used for bone fixation of the hand and foot following trauma or osteotomy. The titanium solid bone screws are a non-cannulated, threaded bone screw which is offered in 2.0, 2.5, 3.0, and 3.0mm diameters with lengths of 6 to 50mm. The system includes titanium and stainless steel instruments to facilitate the placement of the screws. Integra® Ti6® Internal Fixation System ASCENSION ORTHOPEDICS, INC.
3 10381780074328 TI6LOPROIMP TI6LOPROIMP The Integra Ti6 Internal Fixation System is comprised of Low Profile screws used The Integra Ti6 Internal Fixation System is comprised of Low Profile screws used for bone fixation of the hand and foot following trauma or osteotomy. The low profile screw is a cannulated, threaded bone screw which is offered in 2.0, 2.5, 3.0 and 4.0 diameters with lengths of 2.0, 2.5, 3.0, and 4.0. The system includes titanium and stainless steel instruments to facilitate the placement of the screws. Integra® Ti6® Internal Fixation System ASCENSION ORTHOPEDICS, INC.
4 10381780074311 TI6HLESSIMP TI6HLESSIMP The Integra Ti6 Internal Fixation System is comprised of Headless screws used fo The Integra Ti6 Internal Fixation System is comprised of Headless screws used for bone fixation of the hand and foot following trauma or osteotomy. The titanium headless screw is a cannulated dual-thread, headless bone screw which is offered in 2.5 and 3.0mm diameters with lengths of 10 to 24mm. The titanium quick snap is a snap-off solid core screw which is offered in 2.0mm and 2.7mm diameters with lengths of 8 to 22mm.The system includes titanium and stainless steel instruments to facilitate the placement of the screws. Integra® Ti6® Internal Fixation System ASCENSION ORTHOPEDICS, INC.
5 10381780074304 TI6DIGITIMP TI6DIGITIMP The Integra Ti6 Internal Fixation System is comprised of Digital screws used for The Integra Ti6 Internal Fixation System is comprised of Digital screws used for bone fixation of the hand and foot following trauma or osteotomy. The Digital Screw is a cannulated, threaded bone screw which is offered in a 2.0mm diameter with lengths of 24 to 50mm. The system includes titanium and stainless steel instruments to facilitate the placement of the screws. Integra® Ti6® Internal Fixation System ASCENSION ORTHOPEDICS, INC.
6 10381780074281 DIGIFUSEIMP2 DIGIFUSEIMP2 The Integra DigiFuse Implant is a one-piece threaded device intended to be impla The Integra DigiFuse Implant is a one-piece threaded device intended to be implanted into the medullary bone of the lesser toes. The implant is offered in several variations consisting of the combination of 2.0mm and 2.5mm, 0° and 10° blades, as well as standard and short blade options. A 2.0mm x 0° mini-blade is also offered for DIP fusions and smaller anatomy. The system includes instruments to facilitate the placement of the implants. All implants are made from Titanium Alloy, and instrumentation is made from titanium and stainless steel. The DigiFuse implant is indicated for the fixation of osteotomies and reconstruction of the lesser phalanges during procedures to correct deformities of the toes and fingers. Integra® DigiFuse® Implant System ASCENSION ORTHOPEDICS, INC.
7 10381780066590 40012 40012 The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to b The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to be inserted between the posterior and middle facets of the subtalar joint, trial implant and the corresponding instrumentation to facilitate insertion. The implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement. The implant is indicated as an internal support in the treatment of flat foot, providing structural support. bioBLOCK® Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
8 10381780066583 040011 040011 The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to b The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to be inserted between the posterior and middle facets of the subtalar joint, trial implant and the corresponding instrumentation to facilitate insertion. The implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement. The implant is indicated as an internal support in the treatment of flat foot, providing structural support. bioBLOCK® Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
9 10381780066576 040010 040010 The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to b The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to be inserted between the posterior and middle facets of the subtalar joint, trial implant and the corresponding instrumentation to facilitate insertion. The implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement. The implant is indicated as an internal support in the treatment of flat foot, providing structural support. bioBLOCK® Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
10 10381780066569 040009 040009 The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to b The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to be inserted between the posterior and middle facets of the subtalar joint, trial implant and the corresponding instrumentation to facilitate insertion. The implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement. The implant is indicated as an internal support in the treatment of flat foot, providing structural support. bioBLOCK® Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
11 10381780066552 040008 040008 The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to b The bioBLOCK Subtalar Implant consists of a soft-threaded implant, designed to be inserted between the posterior and middle facets of the subtalar joint, trial implant and the corresponding instrumentation to facilitate insertion. The implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement. The implant is indicated as an internal support in the treatment of flat foot, providing structural support. bioBLOCK® Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
12 10381780065777 210326 210326 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
13 10381780065760 210324 210324 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
14 10381780065753 210322 210322 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
15 10381780065746 210320 210320 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
16 10381780065739 210318 210318 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
17 10381780065722 210316 210316 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
18 10381780065715 210314 210314 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
19 10381780065708 210312 210312 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
20 10381780065692 210310 210310 The mini Kompressor Compression Screw is a two-piece fixation device intended fo The mini Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
21 10381780065685 210434 210434 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
22 10381780065678 210432 210432 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
23 10381780065661 210430 210430 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
24 10381780065654 210428 210428 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
25 10381780065647 210426 210426 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
26 10381780065630 210424 210424 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
27 10381780065623 210422 210422 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
28 10381780065616 210420 210420 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
29 10381780065609 210418 210418 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
30 10381780065593 210416 210416 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
31 10381780065586 210414 210414 The standard Kompressor Compression Screw is a two-piece fixation device intende The standard Kompressor Compression Screw is a two-piece fixation device intended for the use in the reduction, stabilization, and internal fixation of bone fractures. The 2-piece design incorporates the use of a leading and trailing screw component. The implant utilizes a variance in thread pitch between the leading and trailing portions of the screw to reduce and fix fracture fragments, and is available in a variety of sizes to accommodate various fracture types and sites. Kompressor™ Compression Screw System ASCENSION ORTHOPEDICS, INC.
32 10381780065531 050112 050112 The MBA titanium subtalar implant is cylindrical in shape and incorporates a cen The MBA titanium subtalar implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement of the implant. The implants are indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
33 10381780065524 050110 050110 The MBA titanium subtalar implant is cylindrical in shape and incorporates a cen The MBA titanium subtalar implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement of the implant. The implants are indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
34 10381780065517 050109 050109 The MBA titanium subtalar implant is cylindrical in shape and incorporates a cen The MBA titanium subtalar implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement of the implant. The implants are indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
35 10381780065500 050108 050108 The MBA titanium subtalar implant is cylindrical in shape and incorporates a cen The MBA titanium subtalar implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement of the implant. The implants are indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
36 10381780065494 050106 050106 The MBA titanium subtalar implant is cylindrical in shape and incorporates a cen The MBA titanium subtalar implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement of the implant. The implants are indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
37 10381780064640 RFOOTIMP RFOOTIMP The Integra Total Foot System is a system containing bone plates and screws desi The Integra Total Foot System is a system containing bone plates and screws designed for use in the skeletally mature foot. The plates and screws are intended to be used for stabilization and fixation of fresh fractures, intra-articular and extra-articular fractures, joint depression and multi-fragmentary fractures. The subject devices can also be used in revision procedures, joint fusion, and in reconstructing the small bones of the feet. Implants are manufactured from Titanium Alloy. The rear foot plates include lapidus plates, interpositioning plates, universal rear foot plates, rear foot reconstruction plates, flat line arthrodesis plates, dwyer displacement plates, calcaneus plates, and fibular plates. Also included are 3.7mm locking screws. Integra® Total Foot System" ASCENSION ORTHOPEDICS, INC.
38 10381780064633 FFMFOOTIMP FFMFOOTIMP The Integra Total Foot System is a system containing bone plates and screws desi The Integra Total Foot System is a system containing bone plates and screws designed for use in the skeletally mature foot. The plates and screws are intended to be used for stabilization and fixation of fresh fractures, intra-articular and extra-articular fractures, joint depression and multi-fragmentary fractures. The subject devices can also be used in revision procedures, joint fusion, and in reconstructing the small bones of the feet. Implants are manufactured from Titanium Alloy. . The fore foot and mid foot plates include open wedge plates, universal forefoot plates, MPJ fusion plates, and tarsalis plates. Also included are 2.7mm locking screws. Integra® Total Foot System" ASCENSION ORTHOPEDICS, INC.
39 10381780064619 HEADHNDSET HEADHNDSET The Headed Compression Screw System contains compression screws used with the An The Headed Compression Screw System contains compression screws used with the Ankle Fusion Plating System. This set includes screws with diamter 6.5mm or 7.5mm. Integra Stainless Headed Compression Screw System ASCENSION ORTHOPEDICS, INC.
40 10381780064602 HEADMIDSET HEADMIDSET The Headed Compression Screw System contains compression screws used with the An The Headed Compression Screw System contains compression screws used with the Ankle Fusion Plating System. This set includes screws with diameter 4.0mm or 4.5mm Integra Stainless Headed Compression Screw System ASCENSION ORTHOPEDICS, INC.
41 10381780064596 TFSREARFTIMP TFSREARFTIMP The Integra Total Foot System is a system containing bone plates and screws desi The Integra Total Foot System is a system containing bone plates and screws designed for use in the skeletally mature foot. The plates and screws are intended to be used for stabilization and fixation of fresh fractures, intra-articular and extra-articular fractures, joint depression and multi-fragmentary fractures. The subject devices can also be used in revision procedures, joint fusion, and in reconstructing the small bones of the feet. Implants are manufactured from Titanium Alloy. The instrumentation is manufactured from biocompatible materials. The rear foot plates include lapidus plates, interpositioning plates, universal rear foot plates, rear foot reconstruction plates, flat line arthrodesis plates, dwyer displacement plates, calcaneus plates, and fibular plates. Integra® Total Foot System" ASCENSION ORTHOPEDICS, INC.
42 10381780064589 TFSFOREFTIMP TFSFOREFTIMP The Integra Total Foot System is a system containing bone plates and screws desi The Integra Total Foot System is a system containing bone plates and screws designed for use in the skeletally mature foot. The plates and screws are intended to be used for stabilization and fixation of fresh fractures, intra-articular and extra-articular fractures, joint depression and multi-fragmentary fractures. The subject devices can also be used in revision procedures, joint fusion, and in reconstructing the small bones of the feet. Implants are manufactured from Titanium Alloy. The instrumentation is manufactured from biocompatible materials. The fore foot plates include open wedge plates, universal forefoot plates, MPJ fusion plates, and tarsalis plates. Integra® Total Foot System" ASCENSION ORTHOPEDICS, INC.
43 10381780064572 TARSALISIMP TARSALISIMP The Integra Total Foot System is a system containing bone plates and screws desi The Integra Total Foot System is a system containing bone plates and screws designed for use in the skeletally mature foot. The plates and screws are intended to be used for stabilization and fixation of fresh fractures, intra-articular and extra-articular fractures, joint depression and multi-fragmentary fractures. The subject devices can also be used in revision procedures, joint fusion, and in reconstructing the small bones of the feet. Implants are manufactured from Titanium Alloy. The instrumentation is manufactured from biocompatible materials. The 2-Hole Straight Tarsalis Plate is offered in short and long lengths. The 3-Hole and 10-Hole Straight Plates are included in the system as standard lengths. The 4-Hole Straight Tarsalis Plate is offered in both standard and short lengths. The Crescentic Tarsalis Plate is offered in left and right configurations. The 4-Hole Diamond Plate is available in left and right configurations. The T-Shaped Tarsalis Plates are offered in 4-hole, 5-hole, and 6-hole configurations. The 5-hole designs are provided in straight, left, and right configurations. The 6-hole is only provided in straight configuration. Upon request, the 6-hole, 7-hole and 8-hole T-Shaped Tarsalis Plates are available. Integra® Total Foot System" ASCENSION ORTHOPEDICS, INC.
44 10381780064558 HITORQ7IMP HITORQ7IMP The Capture High-Torque Screw System consists of various sizes of cannulated scr The Capture High-Torque Screw System consists of various sizes of cannulated screws. The screws are machined, metallic screws with a cannulation that are self-drilling and self-tapping. Each type is offered in a variety of diameters and lengths and is manufactured from stainless steel and titanium. The system is intended for fixation of fractures in long bones, fixation of small bones, arthrodesis of the foot, wrist and elbow, and small and long bone osteotomies. This particular system consists of 7.0mm screws. Instruments are provided to assist with the implants. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
45 10381780064541 HITORQ45IMP HITORQ45IMP The Capture High-Torque Screw System consists of various sizes of cannulated scr The Capture High-Torque Screw System consists of various sizes of cannulated screws. The screws are machined, metallic screws with a cannulation that are self-drilling and self-tapping. Each type is offered in a variety of diameters and lengths and is manufactured from stainless steel and titanium. The system is intended for fixation of fractures in long bones, fixation of small bones, arthrodesis of the foot, wrist and elbow, and small and long bone osteotomies. This particular system consists of 4.0mm and 5.0mm screws. Instruments are provided to assist with the implants. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
46 10381780064534 HITORQ23IMP HITORQ23IMP The Capture High-Torque Screw System consists of various sizes of cannulated scr The Capture High-Torque Screw System consists of various sizes of cannulated screws. The screws are machined, metallic screws with a cannulation that are self-drilling and self-tapping. Each type is offered in a variety of diameters and lengths and is manufactured from stainless steel and titanium. The system is intended for fixation of fractures in long bones, fixation of small bones, arthrodesis of the foot, wrist and elbow, and small and long bone osteotomies. This particular system consists of 2.0mm and 3.0mm screws. Instruments are provided to assist with the implants. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
47 10381780064527 CAPLOPROIMP CAPLOPROIMP The Capture Screw System is comprised of Low Profile screws used for bone fixati The Capture Screw System is comprised of Low Profile screws used for bone fixation of the hand and foot, following trauma or osteotomy. All screws are made from Titanium Alloy, and instrumentation is made from titanium and stainless steel. The low profile, cannulated screw is a cannulated, threaded bone screw which is offered in 2.0, 2.5, 3.0, and 4.0mm diameters with lengths of 6 – 50mm. The system includes instruments to facilitate the placement of the screws. CAPTURE™ Screw System ASCENSION ORTHOPEDICS, INC.
48 10381780064510 CAPHLESSIMP CAPHLESSIMP The Capture Screw System is comprised of headless screws used for bone fixation The Capture Screw System is comprised of headless screws used for bone fixation of the hand and foot, following trauma or osteotomy. All screws are made from Titanium Alloy, and instrumentation is made from titanium and stainless steel. The headless screw is a cannulated, dual-thread headless bone screw which is offered in 2.5 and 3.0mm diameters with lengths of 10 – 34mm. The quick snap screw is a snap-off solid screw which is offered in 2.0mm and 2.7mm diameters with lengths of 8-22mm. The system includes instruments to facilitate the placement of the screws. CAPTURE™ Screw System ASCENSION ORTHOPEDICS, INC.
49 10381780064503 CAPDIGITIMP CAPDIGITIMP The Capture Screw System is comprised of Digital screws used for bone fixation o The Capture Screw System is comprised of Digital screws used for bone fixation of the hand and foot, following trauma or osteotomy. All screws are made from Titanium Alloy, and instrumentation is made from titanium and stainless steel. The Digital Screw is a cannulated, threaded bone screw which is offered in a 2.0mm diameter with lengths of 24 – 50mm. The system includes instruments to facilitate the placement of the screws. CAPTURE™ Screw System ASCENSION ORTHOPEDICS, INC.
50 10381780064497 AFPIMP AFPIMP The Construct Ankle Fusion Plate System consists of two anterior tibia-talus and The Construct Ankle Fusion Plate System consists of two anterior tibia-talus and a lateral tibia-talus-calcaneus arthrodesis plates. The plates are contoured to the peri articular anatomy and have tapered threaded holes which accept compression or locking threaded screws with a major thread diameter of 4.5 or 6.5mm. All plates and screws are manufactured from stainless steel or titanium. The system is intended for arthrodesis of the ankle joint and distal tibia, fractures, osteotomies, fusions, and replantation of small bones in the foot and ankle. Instruments are provided. Construct® Ankle Fusion Plate System ASCENSION ORTHOPEDICS, INC.