Medical Device Recalls
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1 result found
510(K) Number: K150801 |
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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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Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatica... | 2 | 06/09/2016 | Stryker Instruments Div. of Stryker Corporation |
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