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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K062310
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FDA Recall
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Stryker Reflex Hybrid Screw Extractor Inner Shaft; Not Sterile; Manufactured by: Stryker Spine SAS... 2 04/12/2010 Stryker Spine
Stryker Reflex Hybrid Screw Extractor; Not Sterile: Manufactured by: Stryker Spine SAS, Cestas, Fr... 2 04/12/2010 Stryker Spine
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