Medical Device Recalls
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1 result found
510(K) Number: K113756 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2 | 2 | 01/02/2024 | Encore Medical, LP |
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