Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K991807 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Custom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1. Noninflammatory deg... | 2 | 12/17/2020 |
FEI # 1825034 Biomet, Inc. |
| Low Profile Self-Tapping Bone Screw, 6.5 mm X 25 mm, Qty. 1, Biomet Orthopedics, 66 East Bell Drive,... | 2 | 05/03/2011 |
FEI # 1825034 Biomet, Inc. |
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