Medical Device Recalls
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1 result found
510(K) Number: K191146 |
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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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| Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210 | 2 | 01/29/2024 |
FEI # 3014128390 FX SHOULDER |
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