Medical Device Recalls
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1 result found
510(K) Number: K131409 |
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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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PSI Knee System- Prosthesis, knee patellofemorotibial, semi-constrained, cemented, polymer/meal/poly... | 2 | 12/16/2014 | Zimmer CAS |
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