No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 10855068008621 | RLI-002 | RLI-002 | Stainless steel, ring-shaped device that may be added to the Inserter/Extractor. Stainless steel, ring-shaped device that may be added to the Inserter/Extractor. The addition of this device provides an additional level of robustness to the mechanism that attaches the inserter to the CurvaFix Implant | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Ring Lock, Long Inserter |
2 | 10855068008492 | CIA-002 | CIA-002 | Reusable surgical instrument used to engage the proximal end of the flexible Cur Reusable surgical instrument used to engage the proximal end of the flexible CurvaFix® IM Implant in preparation for insertion into the intramedullary canal for implantation. Instrument can also be used to engage the implant during a removal procedure. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Inserter/Extractor |
3 | 10855068008461 | CSS-001 | CSS-001 | A hand-held tubular surgical tool used during a CurvaFix procedure to facilitat A hand-held tubular surgical tool used during a CurvaFix procedure to facilitate the entry of a Guide Pin into the bone. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Spiked Start Sleeve, Cannulated |
4 | 10855068008362 | PQD-001 | PQD-001 | An instrument that enables connection of the torque limiting handle to the Inser An instrument that enables connection of the torque limiting handle to the Inserter during implantation of the CurvaFix IM Implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Quick Disconnect |
5 | 10855068008355 | CIC-002 | CIC-002 | Reusable, stainless steel instrument storage case that is used to contain the im Reusable, stainless steel instrument storage case that is used to contain the implant selection device during sterilization processing in preparation for pelvic fixation procedure. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Sterilization Case, Implant Selection Device |
6 | 10855068008348 | CIA-001 | CIA-001 | Reusable surgical instrument used to engage the proximal end of the flexible Cur Reusable surgical instrument used to engage the proximal end of the flexible CurvaFix® IM Implant in preparation for insertion into the intramedullary canal for implantation. If needed, device can also be used to engage the implant during a removal procedure. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Inserter/Extractor |
7 | 10855068008591 | RLI-001 | RLI-001 | Stainless steel, ring-shaped device that may be added to the Inserter/Extractor. Stainless steel, ring-shaped device that may be added to the Inserter/Extractor. The addition of this device provides an additional level of robustness to the mechanism that attaches the inserter to the CurvaFix Implant | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Ring Lock, Inserter |
8 | 10855068008485 | CCB-002 | CCB-002 | A T-handled instrument used to manually enlarge the diameter of the proximal po A T-handled instrument used to manually enlarge the diameter of the proximal portion of bone canal in preparation for insertion of the CurvaFix Implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Countersink |
9 | 10855068008478 | CGS-002 | CGS-002 | A hand-held stainless steel tube used during a CurvaFix procedure to facilitate A hand-held stainless steel tube used during a CurvaFix procedure to facilitate the acceptance of a guidewire into the bone. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Steerable Guide Sleeve |
10 | 10855068008225 | CGS-001 | CGS-001 | A hand-held tubular surgical device designed to be used during an CurvaFix Impla A hand-held tubular surgical device designed to be used during an CurvaFix Implant implantation procedure to facilitate the acceptance of a Steerable Guide through it. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Steerable Guide Sleeve |
11 | 10855068008218 | CCB-001 | CCB-001 | A manual rotary tool used to enlarge the diameter of the proximal portion of bon A manual rotary tool used to enlarge the diameter of the proximal portion of bone canal in preparation for insertion of the CurvaFix Implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Countersink |
12 | 10855068008157 | CGP-001 | CGP-001 | A wire used to make the initial entry into the pelvic bone in the intended locat A wire used to make the initial entry into the pelvic bone in the intended location and angle for the CurvaFix Implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 2.8 MM Guide Pin |
13 | 10855068008515 | GPT-001 | GPT-001 | A threaded guidewire used to make the initial entry into the pelvic bone in the A threaded guidewire used to make the initial entry into the pelvic bone in the intended location and angle for the CurvaFix Implant. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Guide Pin, 2.8mm Threaded |
14 | 10855068008447 | CTS-001 | CTS-001 | A hand-held stainless steel tube used during a CurvaFix procedure to maintain di A hand-held stainless steel tube used during a CurvaFix procedure to maintain direct access to the surgical site, protect the patient soft tissue, and facilitate the acceptance of other orthopaedic instrumentation into the surgical site. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Soft Tissue Sleeve |
15 | 10855068008423 | CLA-001 | CLA-001 | Reusable surgical instrument used during pelvic fixation procedure to convert a Reusable surgical instrument used during pelvic fixation procedure to convert a flexible intramedullary implant to a rigid state in order to stabilize and repair a bone fracture. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Lock Activator |
16 | 10855068008409 | CSA-001 | CSA-001 | Reusable surgical instrument used during pelvic fixation procedure to convert a Reusable surgical instrument used during pelvic fixation procedure to convert a flexible intramedullary implant to a rigid state in order to stabilize and repair a bone fracture. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Lock Activator |
17 | 10855068008393 | CIC-001 | CIC-001 | Reusable instrument storage case that is used to contain the reusable instrument Reusable instrument storage case that is used to contain the reusable instruments during sterilization processing in preparation for pelvic fixation procedure. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Instrument Sterilization Case |
18 | 10855068008331 | ISD-001 | ISD-001 | Reusable surgical measurement instrument used when determining the size of the C Reusable surgical measurement instrument used when determining the size of the CurvaFix IM Implant to be used in a pelvic fixation procedure. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Implant Selection Device |
19 | 10855068008317 | CFR-090 | CFR-090 | A surgical drilling instrument (9.0mm diameter) intended to be connected to a st A surgical drilling instrument (9.0mm diameter) intended to be connected to a standard power tool, which is used to open and enlarge the medullary canal for the insertion of the CurvaFix IM Implant during a fracture fixation procedure. This device is cannulated so that it can be fed over a guiding wire that has been placed into the correct position inside the bone prior to operation of the drill. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 9.0MM Flexible Reamer |
20 | 10855068008119 | CGK-001 | CGK-001 | A single use kit, composed of a sterile packaged Steerable Guide, Driving Guidew A single use kit, composed of a sterile packaged Steerable Guide, Driving Guidewire and Exchange Tube, that is used during a surgical procedure for the placement of the CurvaFix IM Implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Guidewire Kit |
21 | 10855068008232 | SGC-001 | SGC-001 | A hand-held manual surgical instrument designed to drive the CurvaFix Steerable A hand-held manual surgical instrument designed to drive the CurvaFix Steerable Guide into the intramedullary space. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | T-Handle Chuck |
22 | 10855068008164 | CHC-001 | CHC-001 | A hand-held stainless steel tube used during a CurvaFix Implant implantation pro A hand-held stainless steel tube used during a CurvaFix Implant implantation procedure to maintain direct access to the surgical site, protect the patient soft tissue, and facilitate the acceptance of orthopaedic instrumentation into the surgical site. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Handled Cannula |
23 | 10855068008300 | CFR-085 | CFR-085 | A surgical drilling instrument (8.5mm diameter) intended to be connected to a st A surgical drilling instrument (8.5mm diameter) intended to be connected to a standard power tool, which is used to open and enlarge the medullary canal for the insertion of the CurvaFix IM Implant during a fracture fixation procedure. This device is cannulated so that it can be fed over a guiding wire that has been placed into the correct position inside the bone prior to operation of the drill. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 8.5MM Flexible Reamer |
24 | 10855068008294 | CFR-080 | CFR-080 | A surgical drilling instrument (8.0mm diameter) intended to be connected to a st A surgical drilling instrument (8.0mm diameter) intended to be connected to a standard power tool, which is used to open and enlarge the medullary canal for the insertion of the CurvaFix IM Implant during a fracture fixation procedure. This device is cannulated so that it can be fed over a guiding wire that has been placed into the correct position inside the bone prior to operation of the drill. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 8.0MM Flexible Reamer |
25 | 10855068008522 | CIS-003 | CIS-003 | A custom engineered set of reusable surgical instruments, housed in a sterilizab A custom engineered set of reusable surgical instruments, housed in a sterilizable storage container, that are used during a CurvaFix surgical procedure. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Instrument Set (Case and Reusable Instruments) |
26 | 10855068008508 | GPS-001 | GPS-001 | A smooth guidewire used to make the initial entry into the pelvic bone in the in A smooth guidewire used to make the initial entry into the pelvic bone in the intended location and angle for the CurvaFix Implant. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Guide Pin, 2.8mm Smooth |
27 | 10855068008386 | CIS-002 | CIS-002 | A custom engineered set consisting of reusable implant selection device, housed A custom engineered set consisting of reusable implant selection device, housed in a sterilizable storage container, that is used during a surgical procedure for the CurvaFix IM Implant. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Implant Selection Device Set |
28 | 10855068008287 | CFR-075 | CFR-075 | A surgical drilling instrument (7.5mm diameter) intended to be connected to a st A surgical drilling instrument (7.5mm diameter) intended to be connected to a standard power tool, which is used to open and enlarge the medullary canal for the insertion of the CurvaFix IM Implant during a fracture fixation procedure. This device is cannulated so that it can be fed over a guiding wire that has been placed into the correct position inside the bone prior to operation of the drill. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 7.5MM Flexible Reamer |
29 | 10855068008270 | CFR-070 | CFR-070 | A surgical drilling instrument (7.0mm diameter) intended to be connected to a st A surgical drilling instrument (7.0mm diameter) intended to be connected to a standard power tool, which is used to open and enlarge the medullary canal for the insertion of the CurvaFix IM Implant during a fracture fixation procedure. This device is cannulated so that it can be fed over a guiding wire that has been placed into the correct position inside the bone prior to operation of the drill. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 7.0MM Flexible Reamer |
30 | 10855068008195 | CCS-102 | CCS-102 | A hand-held tubular surgical device designed to be used during an CurvaFix Impla A hand-held tubular surgical device designed to be used during an CurvaFix Implant implantation procedure to facilitate the acceptance of a Step Drill through it. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 10.2 mm Sleeve |
31 | 10855068008263 | CFR-065 | CFR-065 | A surgical drilling instrument (6.5mm diameter) intended to be connected to a st A surgical drilling instrument (6.5mm diameter) intended to be connected to a standard power tool, which is used to open and enlarge the medullary canal for the insertion of the CurvaFix IM Implant during a fracture fixation procedure. This device is cannulated so that it can be fed over a guiding wire that has been placed into the correct position inside the bone prior to operation of the drill. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | 6.5MM Flexible Reamer |
32 | 10855068008249 | CCH-001 | CCH-001 | A hand-held manual surgical instrument designed to strike the T-Handle to advanc A hand-held manual surgical instrument designed to strike the T-Handle to advance the CurvaFix Steerable Guide into the intramedullary space. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Cannulated Hammer |
33 | 10855068008201 | CSD-001 | CSD-001 | A cannulated drill bit that attaches to a surgical power tool. It is used over a A cannulated drill bit that attaches to a surgical power tool. It is used over a guide pin to make the initial entry into the pelvic bone. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Step Drill |
34 | 10855068008539 | CIC-003 | CIC-003 | Reusable instrument storage case that is used to contain the reusable instrument Reusable instrument storage case that is used to contain the reusable instruments during sterilization processing in preparation for pelvic fixation procedure. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Sterilization Case, Outer |
35 | 10855068008430 | CTH-002 | CTH-002 | A surgical instrument that allows a surgeon to insert the CurvaFix IM Implant in A surgical instrument that allows a surgeon to insert the CurvaFix IM Implant into the pelvis without exerting excess torque or force on the implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Torque Limiting Handle |
36 | 10855068008379 | CTH-001 | CTH-001 | A surgical instrument that allows a surgeon to insert the CurvaFix IM Implant in A surgical instrument that allows a surgeon to insert the CurvaFix IM Implant into the pelvis without exerting excess torque or force on the implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Torque Limiting Handle |
37 | 10855068008102 | 9.5 MM x 210 MM, Self Tapping | CRS-095-210-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
38 | 10855068008096 | 9.5 MM x 200 MM, Self Tapping | CRS-095-200-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
39 | 10855068008089 | 9.5 MM x 190 MM, Self Tapping | CRS-095-190-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
40 | 10855068008072 | 9.5 MM x 180 MM, Self Tapping | CRS-095-180-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
41 | 10855068008065 | 9.5 MM x 170 MM, Self Tapping | CRS-095-170-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
42 | 10855068008058 | 9.5 MM x 160 MM, Self Tapping | CRS-095-160-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
43 | 10855068008041 | 9.5 MM x 150 MM, Self Tapping | CRS-095-150-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
44 | 10855068008034 | 9.5 MM x 140 MM, Self Tapping | CRS-095-140-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
45 | 10855068008027 | 9.5 MM x 130 MM, Self Tapping | CRS-095-130-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
46 | 10855068008010 | 9.5 MM x 120 MM, Self Tapping | CRS-095-120-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
47 | 10855068008003 | 9.5 MM x 110 MM, Self Tapping | CRS-095-110-02 | The CurvaFix® IM Implant is an implantable intramedullary device for the fixatio The CurvaFix® IM Implant is an implantable intramedullary device for the fixation of pelvic fractures. It has a threaded, self-tapping distal end, and a proximal end feature for driving torque, and a lock feature that changes the IM Implant from a flexible to rigid state during implantation. The device is manufactured from Stainless Steel. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | CurvaFix® IM Implant |
48 | 10855068008584 | CAT-001 | CAT-001 | A hand-held, stainless steel, tubular device placed into the proximal end of the A hand-held, stainless steel, tubular device placed into the proximal end of the CurvaFix Implant during removal to aid in proper reattachment of the Inserter/Extractor to the implant. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Cannulated Alignment Tube |
49 | 10855068008454 | CDS-001 | CDS-001 | A hand-held tubular surgical device designed to be used during an CurvaFix Impla A hand-held tubular surgical device designed to be used during an CurvaFix Implant implantation procedure to facilitate the acceptance of a Step Drill through it. | HSB,HWC | Rod, Fixation, Intramedullary And Accessories,Screw, Fixation, Bone | 2 | Drill Sleeve |
50 | 10855068008416 | CIS-001 | CIS-001 | A custom engineered set of reusable surgical instruments, housed in a sterilizab A custom engineered set of reusable surgical instruments, housed in a sterilizable storage container, that are used during a surgical procedure for the CurvaFix IM Implant. | HWC,HSB | Screw, Fixation, Bone,Rod, Fixation, Intramedullary And Accessories | 2 | Instrument Set |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 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 |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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 |
15 | 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 |
16 | 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 |
17 | 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 |
18 | 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 |
19 | 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 |
20 | 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 |
21 | 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 |
22 | 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 |
23 | 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 |
24 | 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 |
25 | 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 |
26 | 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 |
27 | 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 |
28 | 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 |
29 | 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 |
30 | 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 |
31 | 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 |
32 | 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 |
33 | 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 |
34 | 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 |
35 | 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 |
36 | 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 |
37 | 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. | HyProCure II Sinus Tarsi Stent Size 06 | GRAMEDICA |
38 | 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. | Guide Wire | GRAMEDICA |
39 | 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. | HyProCure Size 10 | GRAMEDICA |
40 | M621HYP090 | HYP-09 | HYP-09 | HyProCure Sinus Tarsi Implant Size 09. Indications: HyProCure is a talotars HyProCure Sinus Tarsi Implant Size 09. 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 Size 09 | GRAMEDICA |
41 | 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. | HyProCure Size 08 | GRAMEDICA |
42 | M621HYP070 | HYP-07 | HYP-07 | HyProCure Sinus Tarsi Implant Size 07. Indications: HyProCure is a talotar HyProCure Sinus Tarsi Implant Size 07. 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 Size 07 | GRAMEDICA |
43 | M621HYP060 | HYP-06 | HYP-06 | HyProCure Sinus Tarsi Implant Size 06. Indications: HyProCure is a talotarsal HyProCure Sinus Tarsi Implant Size 06. 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 Size 06 | GRAMEDICA |
44 | 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. | HyProCure Size 05 | GRAMEDICA |
45 | M621HD5FG0 | HD-5-FG | HD-5-FG | HyProCure Driver. Reusable instrument, for use with the HyProCure Sinus Tarsi HyProCure Driver. 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. | HyProCure Driver | GRAMEDICA |
46 | M621GM504300 | GM-504-30 | GM-504-30 | 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. | osteo-WEDGE2 30 Degree Angulated Bone Plate Implant, Large | GRAMEDICA |
47 | M621GM504270 | GM-504-27 | GM-504-27 | 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. | osteo-WEDGE2 27 Degree Angulated Bone Plate Implant, Large | GRAMEDICA |
48 | M621GM504240 | GM-504-24 | GM-504-24 | 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. | osteo-WEDGE2 24 Degree Angulated Bone Plate Implant, Large | GRAMEDICA |
49 | M621GM504210 | GM-504-21 | GM-504-21 | 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. | osteo-WEDGE2 21 Degree Angulated Bone Plate Implant, Large | GRAMEDICA |
50 | 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. | osteo-WEDGE2 18 Degree Angulated Bone Plate Implant, Large | GRAMEDICA |