Other products from "MEDTRONIC PS MEDICAL, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00643169474932 91101 CATHETER 91101 VENTRICULAR ANTIMICROBIAL JXG Shunt, central nervous system and components 2 ARES™
2 00643169010697 46856 ASSY 46856 FP-STRATA 2 SHUNT SML JXG Shunt, central nervous system and components 2 Strata®
3 00613994804631 42856 VALVE 42856 FP-STRATA 2 SMALL JXG Shunt, central nervous system and components 2 Strata®
4 00643169975958 46856 ASSY 46856 FP-STRATA 2 SHUNT SML JXG Shunt, central nervous system and components 2 Strata™
5 00763000030155 44000 INLET 44000 VENTRICULAR PORT BOTTOM LKG Port & catheter, implanted, subcutaneous, intraventricular 2 N/A
6 00763000030100 27740 SHUNT 27740 STRATA NSC SNAP REG 120CM JXG Shunt, central nervous system and components 2 Strata®
7 00763000027490 46866 ASSY 46866 FP-STRATA 2 SHUNT REG JXG Shunt, central nervous system and components 2 Strata®
8 00885074204574 45807 CARD 45807 SMART STRATA JXG Shunt, central nervous system and components 2 Strata®
9 00763000624743 46911 BAG 46911 DRAINAGE DEHP-FREE 1PK GWM,JXG Device, monitoring, intracranial pressure,Shunt, central nervous system and components 2 Duet®
10 00763000428778 46916 EDMS 46916 DUET BLUECORE WITH VCATH JXG,GWM,PCB Shunt, central nervous system and components,Device, monitoring, intracranial pr Shunt, central nervous system and components,Device, monitoring, intracranial pressure,External cerebrospinal fluid (CSF) diversion 2 Duet®
11 00763000406097 27304 KIT 27304 EDM LUMBAR DRAINAGE CLOSED GWN,GWM,JXG NYSTAGMOGRAPH,Device, monitoring, intracranial pressure,Shunt, central nervous s NYSTAGMOGRAPH,Device, monitoring, intracranial pressure,Shunt, central nervous system and components 2 N/A
12 00763000395995 27703 EDM CATH 27703 NUM LENGTH MARK 35CM GWM,JXG Device, monitoring, intracranial pressure,Shunt, central nervous system and components 2 N/A
13 00763000395988 27303 EDM LUMBAR 27303 DRAIN KIT OPEN TIP JXG,GWM Shunt, central nervous system and components,Device, monitoring, intracranial pressure 2 N/A
14 00763000343217 27304 KIT 27304 EDM LUMBAR DRAINAGE CLOSED JXG,GWM Shunt, central nervous system and components,Device, monitoring, intracranial pressure 2 N/A
15 00763000333546 27673 KIT 27673 EXACTA W/EDM VCATH BIOGL 35CM JXG,GWM Shunt, central nervous system and components,Device, monitoring, intracranial pressure 2 Exacta™
16 00763000333423 24146 EDMS 24146 BECKER NO Y-SITE GWM,JXG Device, monitoring, intracranial pressure,Shunt, central nervous system and components 2 Becker®
17 00763000169893 46918 EDMS 46918 CLEAR-SITE LASER LEVEL JXG,GWM Shunt, central nervous system and components,Device, monitoring, intracranial pressure 2 Clear-Site®
18 00763000169886 27613 LASER 27613 EXACTA W/SCREW ASSY JXG,GWM Shunt, central nervous system and components,Device, monitoring, intracranial pressure 2 Laser Level
19 00763000063979 PM800N-R MOTOR PM800N-R MR8 PNEUM NAVIGATED RFRB HAW Neurological stereotaxic Instrument 2 MR8 Stealth-Midas
20 00763000063962 PM800-R MOTOR PM800-R MR8 PNEUMATIC REFURB ERL,HBB DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE,MOTOR, DRILL, PNEUMATIC 2 Midas Rex MR8
21 00763000063818 MR8-AVA12DK-R ATT MR8-AVA12DK-R MR8 12CM VRBL AG DKRFB HBE DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) 2 Midas Rex MR8
22 00763000029494 5005 E CATH 5005 E VENT RT ANGLE STD 5CM JXG Shunt, central nervous system and components 2 N/A
23 00763000063726 MR8-AT10ADK-R ATT MR8-AT10ADK-R MR8 TEL BSE ANG DK RFB HBE DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) 2 Midas Rex MR8
24 00763000029067 44211 KIT 44211 VENTRICULOSTOMY RES 6MM SHW JXG Shunt, central nervous system and components 2 N/A
25 00763000029005 96665 SHUNT 96665 STRATA NSC ASSY REG BIOGLIDE JXG Shunt, central nervous system and components 2 Strata®
26 00763000063450 MR8-AA14DK-R ATT MR8-AA14DK-R MR8 14CM ANG DK3.2MMRFB HBE DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) 2 Midas Rex MR8
27 00763000063405 MR8-AA10-R ATT MR8-AA10-R MR8 10CM ANGLD 2.4MM RFRB HBE DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) 2 Midas Rex MR8
28 00763000028534 41408 CATHETER 41408 CSF-VENT STD W/SNAP 8CM LKG Port & catheter, implanted, subcutaneous, intraventricular 2 N/A
29 00763000031398 46837 SHUNT 46837 STRATA II BURR HOLE JXG Shunt, central nervous system and components 2 Strata®
30 00763000031381 46636 SHUNT 46636 STRATA NSC BURR JXG Shunt, central nervous system and components 2 Strata®
31 00763000031275 27186 NEEDLE 27186 TUOHY 14-GAUGE 12CM JXG Shunt, central nervous system and components 2 N/A
32 00763000031268 48405 PASSER 48405 CATH V/P SUBCUT 60CM GYK Instrument, shunt system implantation 1 N/A
33 00763000031237 42836 VALVE 42836 STRATA II BURR HOLE JXG Shunt, central nervous system and components 2 Strata™
34 00763000031084 9013 A RESERVOIR 9013 A VENT 12MM CONVT IC 50MM JXG Shunt, central nervous system and components 2 N/A
35 00763000030599 24106 E RES 24106 E NEONATE ANGUL CATH 7CM JXG Shunt, central nervous system and components 2 N/A
36 00763000030445 22101 C RES 22101 C NEO FLAT DOME W/ 2.5CM VCATH JXG Shunt, central nervous system and components 2 N/A
37 00763000030308 43551 CATH 43551 C/P STD PLIANT BAR IMP JXG Shunt, central nervous system and components 2 N/A
38 00763000030285 44105 RESERVOIR 44105 B/INLET VENT. CONV LKG Port & catheter, implanted, subcutaneous, intraventricular 2 N/A
39 00763000428747 46913 EDMS 46913 DUET INTERLINK SITES PCB,GWM,JXG External cerebrospinal fluid (CSF) diversion,Device, monitoring, intracranial pr External cerebrospinal fluid (CSF) diversion,Device, monitoring, intracranial pressure,Shunt, central nervous system and components 2 Duet®
40 00885074278896 27831 SHUNT 27831 SNAP STRATA II REG BLUNT P/C JXG Shunt, central nervous system and components 2 Strata®
41 00673978248660 5005 I CATH 5005 I VENT RIGHT ANGLE 8CM JXG Shunt, central nervous system and components 2 NA
42 00643169975897 44465 VALVE 44465 STRATA NSC LP JXG Shunt, central nervous system and components 2 Strata™
43 00643169507494 3008 A CLIP 3008 A RIGHT ANGLE SMALL JXG Shunt, central nervous system and components 2 NA
44 00643169497535 24106 B RES 24106 B NEONATE R/A V-CATH 4CM IMP JXG Shunt, central nervous system and components 2 NA
45 00613994965547 27211 CATH 27211 VENT SLOTTED 16CM JXG Shunt, central nervous system and components 2 NA
46 00763000030124 27695 CATH 27695 EDM VENT TRANS W/STRIPE 35CM JXG Shunt, central nervous system and components 2 N/A
47 00763000030018 41103 CATH 41103 CSF-VENT STANDARD PLIANT JXG Shunt, central nervous system and components 2 N/A
48 00885074228273 018051 SCREW 018051 CRUCIATE RESCUE 1.8X5MM 1 HWC Screw, fixation, bone 2 TiMesh®
49 00885074228266 018031 SCREW 018031 CRUCIATE RESCUE 1.8X3MM 1 HWC Screw, fixation, bone 2 TiMesh®
50 00763000029630 23067 ADAPTER 23067 PREIMPLANT TEST SNAP ASSY LKG Port & catheter, implanted, subcutaneous, intraventricular 2 N/A
Other products with the same Product Code "HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M684180803071 18080307 18080307 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 5.0cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
2 M684180803061 18080306 18080306 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 4.5cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
3 M68418080305WD1 18080305WD 18080305WD CANCL 6.5MM BONE SCREW 4.0CM SELF TAPPING IMPLANT PARTNERS™ Implant Partners MICROPORT ORTHOPEDICS INC.
4 M684180803051 18080305 18080305 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 4.0cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
5 M68418080304WD1 18080304WD 18080304WD CANCL 6.5MM BONE SCREW 3.5CM SELF TAPPING IMPLANT PARTNERS™ Implant Partners MICROPORT ORTHOPEDICS INC.
6 M684180803041 18080304 18080304 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 3.5cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
7 M68418080303WD1 18080303WD 18080303WD CANCL 6.5MM BONE SCREW 3.0CM SELF TAPPING IMPLANT PARTNERS™ Implant Partners MICROPORT ORTHOPEDICS INC.
8 M684180803031 18080303 18080303 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 3.0cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
9 M68418080302WD1 18080302WD 18080302WD CANCL 6.5MM BONE SCREW 2.5CM SELF TAPPING IMPLANT PARTNERS™ Implant Partners MICROPORT ORTHOPEDICS INC.
10 M684180803021 18080302 18080302 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 2.5cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
11 M68418080301WD1 18080301WD 18080301WD CANCL 6.5MM BONE SCREW 2.9CM SELF TAPPING IMPLANT PARTNERS™ Implant Partners MICROPORT ORTHOPEDICS INC.
12 M684180803011 18080301 18080301 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 2.0cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
13 M68418080300WD1 18080300WD 18080300WD CANCL 6.5MM BONE SCREW 1.5CM SELF TAPPING IMPLANT PARTNERS™ Implant Partners MICROPORT ORTHOPEDICS INC.
14 M684180803001 18080300 18080300 CANCELLOUS 6.5MM SELF-TAPPING BONE SCREW 1.5cm LENGTH Advantim MICROPORT ORTHOPEDICS INC.
15 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. osteo-WEDGE 3.0mm x 26mm Locking Bone Screw GRAMEDICA
16 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. osteo-WEDGE 3.0mm x 24mm Locking Bone Screw GRAMEDICA
17 M621OW30LBS22MM0 GM-500-22 OW3.0LBS-22MM osteo-WEDGE 3.0mm x 22mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm 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. osteo-WEDGE 3.0mm x 22mm Locking Bone Screw GRAMEDICA
18 M621OW30LBS20MM0 GM-500-20 OW3.0LBS-20MM osteo-WEDGE 3.0mm x 20mm Locking Bone Screw. For use with the osteo-WEDGE Openi osteo-WEDGE 3.0mm x 20mm Locking Bone Screw. 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. osteo-WEDGE 3.0mm x 20mm Locking Bone Screw GRAMEDICA
19 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. osteo-WEDGE 3.0mm x 18mm Locking Bone Screw GRAMEDICA
20 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. osteo-WEDGE 3.0mm x 16mm Locking Bone Screw GRAMEDICA
21 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. osteo-WEDGE 3.0mm x 14mm Locking Bone Screw GRAMEDICA
22 M621OW30LBS12MM0 GM-500-12 OW3.0LBS-12MM osteo-WEDGE 3.0mm x 12mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm 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. osteo-WEDGE 3.0mm x 12mm Locking Bone Screw GRAMEDICA
23 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. osteo-WEDGE 3.0mm x 10mm Locking Bone Screw GRAMEDICA
24 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. osteo-WEDGE 3.0mm x 08mm Locking Bone Screw GRAMEDICA
25 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. osteo-WEDGE 2.5mm x 22mm Locking Bone Screw GRAMEDICA
26 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. osteo-WEDGE 2.5mm x 20mm Locking Bone Screw GRAMEDICA
27 M621OW25LBS18MM0 GM-200-18 OW2.5LBS-18MM osteo-WEDGE 2.5mm x 18mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm 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. osteo-WEDGE 2.5mm x 18mm Locking Bone Screw GRAMEDICA
28 M621OW25LBS16MM0 GM-200-16 OW2.5LBS-16MM osteo-WEDGE 2.5mm x 16mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm 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. osteo-WEDGE 2.5mm x 16mm Locking Bone Screw GRAMEDICA
29 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. osteo-WEDGE 2.5mm x 14mm Locking Bone Screw GRAMEDICA
30 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. osteo-WEDGE 2.5mm x 12mm Locking Bone Screw GRAMEDICA
31 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. osteo-WEDGE 2.5mm x 10mm Locking Bone Screw GRAMEDICA
32 M621OW25LBS08MM0 GM-200-08 OW2.5LBS-08MM osteo-WEDGE 2.5mm x 08mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm 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. osteo-WEDGE 2.5mm x 08mm Locking Bone Screw GRAMEDICA
33 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. osteo-WEDGE Temporary Tack 2.4mm x 12mm GRAMEDICA
34 M621HYPINSTRAY0 HYP-INS-TRAY HYP-INS-TRAY HyProCure (reusable) Instrument Set. The instrument set contains six Trial Sizer HyProCure (reusable) Instrument Set. The instrument set contains six Trial Sizers (05mm thru 10mm), one Driver and three Guide Wires. 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. HyProCure Instrument Set GRAMEDICA
35 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. HyProCure II Trial Sizer 12 GRAMEDICA
36 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.. HyProCure II Trial Sizer 11 GRAMEDICA
37 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. HyProCure II Trial Sizer 10 GRAMEDICA
38 M621HYPIITS090 HYP II-TS-09 HYP II-TS-09 HyProCure II Trial Sizer 09 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 09 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. HyProCure II Trial Sizer 09 GRAMEDICA
39 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. HyProCure II Trial Sizer 08 GRAMEDICA
40 M621HYPIITS070 HYP II-TS-07 HYP II-TS-07 HyPrHyProCure II Trial Sizer 07 instrument. For use with the HyProCure II Sinus HyPrHyProCure II Trial Sizer 07 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. HyProCure II Trial Sizer 07 GRAMEDICA
41 M621HYPIITS060 HYP II-TS-06 HYP II-TS-06 HyProCure II Trial Sizer 06 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 06 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. HyProCure II Trial Sizer 06 GRAMEDICA
42 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. HyProCure II Positioning Sleeve GRAMEDICA
43 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 HyProCure II Instrument Tray-Set GRAMEDICA
44 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. HyProCure II Driver GRAMEDICA
45 M621HYPII120 HYP II-12 HYP II-12 HyProCure II Sinus Tarsi Implant Size 12. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 12. 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. HyProCure II Sinus Tarsi Stent Size 12 GRAMEDICA
46 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. HyProCure II Sinus Tarsi Stent Size 11 GRAMEDICA
47 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. HyProCure II Sinus Tarsi Stent Size 10 GRAMEDICA
48 M621HYPII090 HYP II-09 HYP II-09 HyProCure II Sinus Tarsi Implant Size 09. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 09. 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. HyProCure II Sinus Tarsi Stent Size 09 GRAMEDICA
49 M621HYPII080 HYP II-08 HYP II-08 HyProCure II Sinus Tarsi Implant Size 08. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 08. 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. HyProCure II Sinus Tarsi Stent Size 08 GRAMEDICA
50 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. HyProCure II Sinus Tarsi Stent Size 07 GRAMEDICA