Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K242273 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix, OsteoSurge 100 Demineralized... | 2 | 01/16/2025 |
FEI # 3001503333 IsoTis OrthoBiologics, Inc. |
| OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01. | 2 | 01/15/2025 |
FEI # 3001503333 IsoTis OrthoBiologics, Inc. |
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