Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K043421 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Product is OPTEFORM Allograft Paste of varying sizes. Product is labeled in part: ''***Processed ... | 3 | 02/07/2006 | Regeneration Technologies, Inc. |
Product is OPTEFORM Allografts of varying sizes. Product is labeled in part: ''***Processed at: Re... | 3 | 02/07/2006 | Regeneration Technologies, Inc. |
Product is RTI Allograft Paste of varying sizes. Product is labeled in part: ''***Processed at: Re... | 3 | 02/07/2006 | Regeneration Technologies, Inc. |
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