Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K142658 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| T7 Driver Solid AO (Part Number 110018541) Product Usage: The Biomet Headless Compression Screws... | 2 | 05/09/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
| T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression S... | 2 | 05/09/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
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