Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K042707 |
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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| Optimum Expanse R Grafton is a human bone allograft product containing demineralized human bone t... | 2 | 10/18/2012 |
FEI # 3002600221 Osteotech Inc |
| Grafton DBM Matrix PLF Multiple Sizes Grafton is a human bone allograft product containing demin... | 2 | 10/18/2012 |
FEI # 3002600221 Osteotech Inc |
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