Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K050882 |
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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. |
Panta® Arthrodesis Nail Support device, 510 (k) #K050882. One (1) unit of product is kitted within ... | 2 | 04/16/2012 | Integra LifeSciences Corp. |
PANTA Nails, 10mm x 150 length, Newdeal, Lyon France; Integra, 311 Enterprise Drive, Plainsboro, NJ.... | 2 | 09/16/2008 | Integra LifeSciences Corp. |
Integra PANTA Arthrodesis Nail System. Intended for use in tibiotalocalcaneal arthrodesis and tr... | 2 | 07/16/2013 | Integra LifeSciences Corporation |
Panta Support Device Panta® Arthrodesis Nail Instrumentation Tray One unit per package. The PANTA... | 2 | 11/02/2010 | Integra LifeSciences Corporation |
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