Medical Device Recalls
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1 result found
510(K) Number: K121713 |
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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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Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy,... | 2 | 06/25/2020 | PROVIDENCE MEDICAL TECHNOLOGIES |
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