Medical Device Recalls
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1 result found
510(K) Number: K012091 |
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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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| PROFEMUR(R) R RASP HANDLE, REF PPW38078, 1 EACH, NON-STERILE, MicroPort Orthopedics, Arlington, TN ... | 2 | 01/03/2017 | MicroPort Orthopedics Inc. |
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