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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ACUMED IMPACT 10CC. Product Number: 65-0110-S, UDI: 813845020269 - Callos is indicated to fill bony... | 2 | 07/15/2020 | Skeletal Kinetics, Llc |
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