Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K062353 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Integra Mosaik Putty, 15cc, Catalog # PTY10256 Integra Lifesciences, Plainsboro, NJ | 2 | 03/06/2009 | Integra LifeSciences Corp |
| Integra OS Osteoconductive Scaffold Putty (2.5 cc and 5 cc). Integra OS Putty, combined with bone ma... | 2 | 02/08/2012 | Integra LifeSciences Corp |
| Integra Mozaik Putty 2.5cc, 5 cc, 10 cc Product Usage: The product is a bone graft substitut... | 2 | 06/12/2012 | Integra LifeSciences Corp. |
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