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U.S. Department of Health and Human Services

510(k) Premarket Notification
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61 to 70 of 117 Results
ProductCode: HRS Applicant: SYNTHES (USA) Decision Date To: 11/28/2022
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Export all 117 Records to ExcelExport to Excel | Download Files | More About 510(k)
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synthes (usa) sternal fixation system SYNTHES (USA) K052683 12/05/2005
synthes (usa) sternal reconstruction system SYNTHES (USA) K031508 05/30/2003
synthes (usa) tomofix medial distal femur plates SYNTHES (USA) K081353 07/23/2008
synthes (usa) variable angle-locking compression plate (va-lcp) distal radius system SYNTHES (USA) K071184 06/22/2007
synthes 1.0mm ti. cortex, self-drilling screws (hand & neuro) SYNTHES (USA) K050607 04/11/2005
synthes 2.4 mm/2.7 mm variable angle lcp forefoot/midfoot system SYNTHES (USA) K100776 08/03/2010
synthes 2.7 mm lc-dcp, 3.5 mm profile SYNTHES (USA) K011170 07/05/2001
synthes 2.7 mm/3.5 mm lcp distal fibula plates SYNTHES (USA) K073460 02/21/2008
synthes 2.7 mm/3.5 mm lcp distal fibula plates SYNTHES (USA) K083213 12/30/2008
synthes 3.0 mm pc-fix system SYNTHES (USA) K981372 05/11/1998
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