| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00190446735922 | 342-13-705 | EMPOWR 3D KNEETM INS, 5R 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 2 | 00190446735915 | 341-13-705 | EMPOWR 3D KNEETM INS, 5L 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 3 | 00190446735762 | 341-11-702 | EMPOWR 3D KNEETM INS, 2L 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 4 | 00190446302636 | 414922 | 2.0 AND 2.7MM SCREW DRIVER HANDLE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | DJO SURGICAL | |
| 5 | 00190446747482 | 800-05-096 | DJO EMPOWR REVISION KNEE, FEMORAL TRIAL LOCATOR, SZ 6-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 6 | 00190446747468 | 800-05-095 | DJO EMPOWR REVISION KNEE, FEMORAL TRIAL LOCATOR, SZ 2-5 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 7 | 00190446745266 | 800-05-094 | DJO EMPOWR REVISION KNEE, FEMORAL FLEXION TOWER 0/3 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 8 | 00190446302605 | 414916 | DISCOVERY XS HUM RES TEMPLATE | HWT | TEMPLATE | 1 | DJO SURGICAL | |
| 9 | 00190446736165 | 342-13-711 | EMPOWR 3D KNEETM INS, 11R 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 10 | 00190446302582 | 414913 | DISCOVERY XS FOSSA REAMER | HTO | REAMER | 1 | DJO SURGICAL | |
| 11 | 00190446736158 | 341-13-711 | EMPOWR 3D KNEETM INS, 11L 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 12 | 00190446302575 | 414912 | DISCOVERY 5 STEP FOSSA REAMER | HTO | REAMER | 1 | DJO SURGICAL | |
| 13 | 00190446736141 | 342-11-711 | EMPOWR 3D KNEETM INS, 11R 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 14 | 00190446736134 | 341-11-711 | EMPOWR 3D KNEETM INS, 11L 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 15 | 00190446736127 | 342-13-710 | EMPOWR 3D KNEETM INS, 10R 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 16 | 00190446736110 | 341-13-710 | EMPOWR 3D KNEETM INS, 10L 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 17 | 00190446302292 | 414868 | DISC 2.5MM RIGHT ULNA RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
| 18 | 00190446736103 | 342-11-710 | EMPOWR 3D KNEETM INS, 10R 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 19 | 00190446302285 | 414867 | DISC 2.5MM LEFT ULNA RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
| 20 | 00190446736097 | 341-11-710 | EMPOWR 3D KNEETM INS, 10L 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 21 | 00190446736080 | 342-13-709 | EMPOWR 3D KNEETM INS, 9R 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 22 | 00190446736073 | 341-13-709 | EMPOWR 3D KNEETM INS, 9L 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 23 | 00190446736066 | 342-11-709 | EMPOWR 3D KNEETM INS, 9R 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 24 | 00190446736059 | 341-11-709 | EMPOWR 3D KNEETM INS, 9L 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 25 | 00190446736042 | 342-13-708 | EMPOWR 3D KNEETM INS, 8R 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 26 | 00190446736035 | 341-13-708 | EMPOWR 3D KNEETM INS, 8L 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
| 27 | 00190446736028 | 342-11-708 | EMPOWR 3D KNEETM INS, 8R 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 28 | 00190446764335 | 803-03-241 | MODULAR T-HANDLE, LINEAR PLUS | LXH | Orthopedic manual surgical instrument | 1 | DJO SURGICAL | |
| 29 | 00190446764274 | 800-99-161 | EMPOWR REVISION KNEE, HALF-TRAY LID | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DJO SURGICAL | |
| 30 | 00190446757672 | 800-99-160 | EMPOWR REVISION KNEE, OUTLIER TRAY, SZ: 2-3, 10-11 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DJO SURGICAL | |
| 31 | 00190446301950 | 414820 | DISC 3.5MM DIST HUMERAL RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
| 32 | 00190446757665 | 800-99-159 | EMPOWR REVISION KNEE, CORE TRAY, SZ: 4-9 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DJO SURGICAL | |
| 33 | 00190446301912 | 414815 | DISC 3.5X124MM PROX HUM RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
| 34 | 00190446754282 | 800-05-098 | DJO EMPOWR REVISION KNEE, STEM EXTENDER TRIAL, 15MM X 25MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 35 | 00190446753957 | 800-05-097 | DJO EMPOWR REVISION KNEE, ANTERIOR CUT GUIDE, SIZE 6-11 | FZX | Guide, surgical, instrument | 1 | DJO SURGICAL | |
| 36 | 00190446750734 | 800-05-093 | DJO EMPOWR REVISION KNEE, 3.5MM BALL END HEX DRIVER | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 37 | 00190446735663 | 800-05-122 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 10/11, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 38 | 00190446735656 | 800-05-121 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 8/9, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 39 | 00190446735649 | 800-05-120 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 6/7, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 40 | 00190446301905 | 414814 | DISC 3.5X84MM PROX HUM RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
| 41 | 00190446735632 | 800-05-119 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 4/5, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 42 | 00190446735625 | 800-05-118 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 2/3, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 43 | 00190446735618 | 800-05-117 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 10/11, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 44 | 00190446735601 | 800-05-116 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 8/9, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 45 | 00190446296652 | 803-42-44K | Trial Liner, EMPOWR Acetabular, 10°, 44K | FZX | Guide, surgical, instrument | 1 | DJO SURGICAL | |
| 46 | 00190446735595 | 800-05-115 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 6/7, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 47 | 00190446735588 | 800-05-114 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 4/5, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 48 | 00190446735571 | 800-05-113 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 2/3, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 49 | 00190446735564 | 800-05-112 | DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 10/11, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
| 50 | 00190446735557 | 800-05-111 | DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 8/9, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 15060155711260 | 234-010-173 | 234-010-173 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 2 | 15060155711253 | 234-010-172 | 234-010-172 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 3 | 15060155711246 | 234-010-168 | 234-010-168 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 4 | 15060155711239 | 234-010-170 | 234-010-170 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 5 | 15060155711222 | 234-010-160 | 234-010-160 | The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorba The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorbable Poly (L-lactic) Acid and Calcium Phosphate which will be gradually resorbed into the body. this function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 6 | 15060155711215 | 3910-200-086 | 3910-200-086 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 7 | 15060155711208 | 3910-200-085 | 3910-200-085 | The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 8 | 15060155711192 | 3910-200-084 | 3910-200-084 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 9 | 15060155711185 | 3910-200-083 | 3910-200-083 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 10 | 15060155711178 | 3910-200-082 | 3910-200-082 | The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 11 | 15060155711161 | 3910-200-081 | 3910-200-081 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 12 | 15060155711154 | 3910-200-080 | 3910-200-080 | The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 13 | 15060155710652 | 160-135T | 160-135T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 14 | 15060155710645 | 160-130T | 160-130T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 15 | 15060155710621 | 160-935T | 160-935T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 16 | 15060155710614 | 160-930T | 160-930T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 17 | 15060155710607 | 160-925T | 160-925T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 18 | 15060155710584 | 160-830T | 160-830T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 19 | 15060155710577 | 160-825T | 160-825T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 20 | 15060155710546 | 160-725T | 160-725T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible and should not be used at an infected site. | Bilok® Screw | BIOCOMPOSITES LTD |
| 21 | 15060155710508 | 160-935ST | 160-935ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
| 22 | 15060155710492 | 160-930ST | 160-930ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
| 23 | 15060155710362 | 234-500-350 | 234-500-350 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
| 24 | 15060155710355 | 234-500-340 | 234-500-340 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
| 25 | 15060155710348 | 234-010-180 | 234-010-180 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 26 | 15060155710331 | 234-010-179 | 234-010-179 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 27 | 15060155710324 | 234-010-178 | 234-010-178 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 28 | 15060155710317 | 234-010-177 | 234-010-177 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 29 | 15060155710300 | 234-010-167 | 234-010-167 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 30 | 15060155710294 | 234-010-166 | 234-010-166 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 31 | 15060155710287 | 234-010-165 | 234-010-165 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 32 | 15060155710270 | 234-010-164 | 234-010-164 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 33 | 15060155710263 | 234-010-163 | 234-010-163 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 34 | 15060155710256 | 234-010-162 | 234-010-162 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 35 | 15060155710249 | 234-010-161 | 234-010-161 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 36 | 14061144348987 | GP001A.076.031.MH | GP001A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 37 | 14053613285541 | OC06D.076.032 | OC06D.076.032.STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
| 38 | 14053613285534 | OC907P.067.032 | OC907P.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 39 | 14053613285329 | GS905.050.032.M5 | GS905.050.032.STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 40 | 14053613285145 | 02-029-99-1004 | 02-029-99-1004 | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 41 | 14053613284780 | GP007.075.032.K4 | GP007.075.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 42 | 14053613284766 | GS901.033.032.K4 | GS901.033.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 43 | 14053613284391 | OC06Z.127.032 | OC06Z.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
| 44 | 14053613284384 | OC04N.127.032 | OC04N.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
| 45 | 14053613284377 | OC06D.067.032 | OC06D.067.032 STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
| 46 | 14053613284223 | GP007A.076.031 | GP007A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 47 | 14053613283837 | OC005.067.032 STE | OC005.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 48 | 14053613282625 | GP003A.027.030.M5 | GP003A.027.030 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 49 | 14053613282601 | OC002A.089.032 STE | OC002A.089.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 50 | 14053613282069 | GP005.067.032.M5 | GP005.067.032 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG |