Medical Device Recalls
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1 result found
510(K) Number: K201321 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| VA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part... | 2 | 03/01/2024 | Synthes (USA) Products LLC |
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