Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K100986 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SKAFFOLD CMF IMPRESS (MP), 5CC. Product Number: CMMP-IM05, UDI: 813845020689 - Product Usage: Callo... | 2 | 07/15/2020 | Skeletal Kinetics, Llc |
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