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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K021458
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Synthes In Situ Bender/Cutter Kit-Wide-Sterile. Catalog Number 530.521S. 2 02/24/2010 FEI # 3005180112
Synthes USA (HQ), Inc.
Synthes InSitu Bender Cutter Kit Wide Sterile Catalog number 530.521S, used with Synthes Rapid Resor... 2 06/01/2009 FEI # 3005180112
Synthes Spine
Synthes InSitu Bender Cutter Kit Narrow Sterile Catalog number 530.522S, used with Synthes Rapid Res... 2 06/01/2009 FEI # 3005180112
Synthes Spine
In Situ Bender Cutter Kit Narrow Sterile, Catalog number 530.522S. Used with Synthes' Rapid Resor... 2 05/21/2009 FEI # 3005180112
Synthes Spine
In Situ Bender Cutter Kit Wide Sterile, Catalog number 530.521S Used with Synthes' Rapid Resorbab... 2 05/21/2009 FEI # 3005180112
Synthes Spine
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