Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K974150 |
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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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Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components directly connected to t... | 2 | 05/04/2020 | Nobel Biocare Usa Llc |
Temporary Abutment Engaging CC RP pre-manufactured prosthetic components directly connected to the e... | 2 | 05/04/2020 | Nobel Biocare Usa Llc |
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