Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K991581 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NexGen LPS-FLEX Option Femoral NexGen LPS-FLEX Precoat Femoral prosthesis, knee, patellofemorotibi... | 2 | 02/22/2016 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEX... | 2 | 03/12/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
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