Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K934469 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Titanium IFS, Item number 909680 - Product Usage: Bone to bone fixation. | 2 | 12/17/2020 |
FEI # 1825034 Biomet, Inc. |
| TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of i... | 2 | 01/30/2013 |
FEI # 1825034 Biomet, Inc. |
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