Medical Device Recalls
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1 result found
510(K) Number: K141551 |
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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 PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigatio... | 2 | 04/19/2017 | Stryker Instruments Div. of Stryker Corporation |
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