Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K123486 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon® Tritanium® Tibi... | 2 | 06/03/2022 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/... | 2 | 03/08/2021 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with Secondary Lock, Non-Sterile, ... | 2 | 08/11/2016 |
FEI # 3003070421 Stryker Howmedica Osteonics Corp. |
| Stryker Orthopaedics, MIS MODULAR DISTAL CAPTURE TRIATHLON MIS INSTRUMENTS, REF 6541-5-723, Lot Admi... | 2 | 11/09/2015 |
FEI # 3003070421 Stryker Howmedica Osteonics Corp. |
| Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon Distal Capture Assembly is ... | 2 | 03/16/2015 |
FEI # 3003070421 Stryker Howmedica Osteonics Corp. |
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