Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K091788 |
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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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Panta Nail, Rx only, Sterile, | 2 | 03/23/2017 | Integra LifeSciences Corp. |
Integra PANTA Arthrodesis Nail System. Intended for use in tibiotalocalcaneal arthrodesis and tr... | 2 | 07/16/2013 | Integra LifeSciences Corporation |
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