Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K912245 |
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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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| Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile Titanium, Accessory to tota... | 2 | 04/04/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
| Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to tota... | 2 | 04/04/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
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