Medical Device Recalls
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1 result found
510(K) Number: K955697 |
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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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Abutment Screw Retrieval Kit - Product Usage: The kit itself does not have a specific intended Use, ... | 2 | 02/19/2020 | Nobel Biocare Usa Llc |
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