Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K100986 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provi... | 2 | 05/29/2020 | Osteomed, LLC |
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