Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K082172 |
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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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stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 6 RM/LL), REF 170616, intended for use in a Partial ... | 2 | 04/12/2023 | Howmedica Osteonics Corp. |
stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615, intended for use in a Partial ... | 2 | 04/12/2023 | Howmedica Osteonics Corp. |
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