Medical Device Recalls
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1 result found
510(K) Number: K121640 |
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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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Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Tibia) is intended to be used as... | 2 | 11/21/2014 | Materialise USA LLC |
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