Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K091321 |
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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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OsteoSelect DBM Putty Product Usage: Orthopedic bone filler | 2 | 04/17/2013 | Bacterin International, Inc. |
Bacterin International, Inc., Osteoselect Demineralized Bone Matrix DMB Putty; Graft ID# B090056-66... | 2 | 02/11/2013 | Bacterin International, Inc. |
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