No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 03661489693489 | 269348 | PHX,KWS,KWT | Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constraine Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | 2 | magnetic pin driver | ||
2 | 03661489691539 | 269153 | PHX,KWT,KWS | Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Non-Constrained Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | fraise glène canulée ronde XL / 50 | ||
3 | 03661489690839 | 269083 | HSB | Rod, Fixation, Intramedullary And Accessories | 2 | Insert CALCANAIL V3 | ||
4 | 03661489686993 | 268699 - ARROW® CEMENTLESS POROUS GLENOID BASE 46-LP | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
5 | 03661489686986 | 268698 - ARROW® CEMENTLESS POROUS GLENOID BASE 44S-LP | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
6 | 03661489677052 | 267705 - ARROW® CEMENTLESS POROUS GLENOID BASE 48 | PHX,KWS,KWT | Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constraine Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
7 | 03661489677045 | 267704 - ARROW® CEMENTLESS POROUS GLENOID BASE 46 | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
8 | 03661489677038 | 267703 - ARROW® CEMENTLESS POROUS GLENOID BASE 44-LP | PHX,KWS,KWT | Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constraine Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
9 | 03661489677021 | 267702 - ARROW® CEMENTLESS POROUS GLENOID BASE 44S | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
10 | 03661489677014 | 267701 - ARROW® CEMENTLESS POROUS GLENOID BASE 44 | PHX,KWS,KWT | Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constraine Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | 2 | ARROW® ANATOMICAL POROUS GLENOID | ||
11 | 03661489676536 | 267653 | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | Bow-tie cannulated reamer 50 | ||
12 | 03661489676512 | 267651 | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | Bow-tie cannulated reamer 46 | ||
13 | 03661489676123 | 267612 | KWS,KWT,PHX | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoul Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | bloc de coupe sup | ||
14 | 03661489676109 | 267610 | KWT,KWS,PHX | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Shoulder Prosthesis, Reverse Configuration | 2 | Cutting Guide Support | ||
15 | 03661489674563 | 267456 | HSB | Rod, Fixation, Intramedullary And Accessories | 2 | COUVERCLE TELEGRAPH V1 | ||
16 | 03661489674419 | 267441 | HSB | Rod, Fixation, Intramedullary And Accessories | 2 | Fraise boule Ø7,9 L110mm | ||
17 | 03661489673634 | 267363 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | FH ANT APP RETRACTOR TRAY | ||
18 | 03661489670558 | 267055 | HSB | Rod, Fixation, Intramedullary And Accessories | 2 | Tréphine filetée Ø10L105 grand AO | ||
19 | 03661489668395 | 266839 | KWT,KWS,MBF | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented | 2 | glenoid reamer handle 50 | ||
20 | 03661489666575 | 266657 | PHX | Shoulder Prosthesis, Reverse Configuration | 2 | ARROW V10 tray n°4 | ||
21 | 03661489663499 | 266349 | HSB | Rod, Fixation, Intramedullary And Accessories | 2 | ancillaire CALCANAIL V2 | ||
22 | 03661489662324 | 266232 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | CHARNLEY RETRACTOR 7,5CM | ||
23 | 03661489662201 | 266220 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | ARROW REPRISE PANIER + COUVERCLE + AMENAGEMENT | ||
24 | 03661489654237 | 265423 | KWT,KWS,MBF | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Should Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented | 2 | guide pin Ø3 L170 | ||
25 | 03661489649370 | 264937 | MBI,HWC | Fastener, Fixation, Nondegradable, Soft Tissue,Screw, Fixation, Bone | 2 | TLS workstation | ||
26 | 03661489645020 | 264502 | KWS,KWT,HSD | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoul Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | 2 | Humeral trial insert Ø42 H05 | ||
27 | 03661489644610 | 264461 | MBF,KWS,KWT | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Sh Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | 2 | Arrow pin extractor | ||
28 | 03661489644597 | 264459 | PHX,KWT,KWS | Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Non-Constrained Shoulder Prosthesis, Reverse Configuration,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | Impactor handle | ||
29 | 03661489610974 | 261097 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | trial humeral insert D36 H05 | ||
30 | 03661489610929 | 261092 | KWS,KWT,HSD | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoul Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | 2 | Glenosphere trial Ø36 | ||
31 | 03661489610912 | 261091 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | trial glenoid base size 50 | ||
32 | 03661489610790 | 261079 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | Glenoid template Ø48 | ||
33 | 03661489610714 | 261071 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | Cemented trial glenoid Ø46 | ||
34 | 03661489610660 | 261066 | KWS,KWT,HSD | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoul Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | 2 | glenoid clamp | ||
35 | 03661489610561 | 261056 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | Pins de fixation pour bloc de coupe | ||
36 | 03661489610530 | 261053 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | Retroversion rod | ||
37 | 03661489610417 | 261041 | KWS,KWT,HSD | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoul Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | 2 | Humeral head sizer Ø40, 44, 46 | ||
38 | 03661489610110 | 261011 | HSD,KWT,KWS | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | 2 | cutting guide support | ||
39 | 03661489573804 | 257380 | MBI,HWC | Fastener, Fixation, Nondegradable, Soft Tissue,Screw, Fixation, Bone | 2 | BROCHE 25CM 2,4MM BOUT MECHE BOUT ROND (Teknomedical) | ||
40 | 03661489573187 | 257318 | KWS,KWT,HSD | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoul Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented,Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | 2 | ARROW INSERT D'ESSAI HUMERAL D39 H10 | ||
41 | 03661489560422 | 256042 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | ESOP HA SIZER Ø12 | ||
42 | 03661489560392 | 256039 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | SMALL CUTTING CHISEL | ||
43 | 03661489560125 | 256012 | MBI,HWC | Fastener, Fixation, Nondegradable, Soft Tissue,Screw, Fixation, Bone | 2 | CoLS workstation U-Handle lever assembly | ||
44 | 03661489558153 | 255815 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | TRIAL HEAD FOR D.8 BROACH D.28 +0 | ||
45 | 03661489558146 | 255814 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | TRIAL HEAD FOR D.8 BROACH D.28 -3,5 | ||
46 | 03661489557934 | 255793 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | ESOP BROACH D8 RIGHT S 11,25 | ||
47 | 03661489557897 | 255789 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | ESOP BROACH D8 LEFT S 20 | ||
48 | 03661489557866 | 255786 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | ESOP BROACH D8 LEFT S 15 | ||
49 | 03661489557835 | 255783 | MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | ESOP BROACH D8 LEFT S 11,25 | ||
50 | 03661489556968 | 255696 | MBI,HWC | Fastener, Fixation, Nondegradable, Soft Tissue,Screw, Fixation, Bone | 2 | Femoral PCL Universal guide |
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 |