Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K153695 |
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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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Zyston® Transform Implant Kit. Model Number PCR8200-3101. Device labeled sterile. | 2 | 08/11/2016 | Zimmer Biomet Spine, Inc |
Zyston® Transform Instrument Case. Model Number PCR8200-2101. Device labeled sterile. | 2 | 08/11/2016 | Zimmer Biomet Spine, Inc |
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