Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061487 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CD... | 2 | 02/24/2022 |
FEI # 3003300673 Collagen Matrix, Inc. |
| RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated as dural substitutes for the repair of dura matt... | 2 | 02/24/2022 |
FEI # 3003300673 Collagen Matrix, Inc. |
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