Medical Device Recalls
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1 result found
510(K) Number: K071373 |
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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 Xia 3 Anti-Torque Key Manual Surgical Instrument; Catalog Number 48237026. Product Us... | 2 | 06/05/2012 | Stryker Spine |
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