Medical Device Recalls
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1 result found
510(K) Number: K051678 |
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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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13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX, sterile -Intended to facilitate tibiotaloca... | 2 | 03/01/2024 | Synthes (USA) Products LLC |
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