Medical Device Recalls
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1 result found
510(K) Number: K180503 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, ... | 2 | 03/30/2021 |
FEI # 3006179046 Nuvasive Specialized Orthopedics Inc |
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