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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 50 Results
ProductCode: JWH Applicant: SMITH & NEPHEW, INC. Decision Date To: 10/16/2021
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510(K)
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profix flex cruciate retaining articular insert SMITH & NEPHEW, INC. K051229 07/20/2005
legion cobalt chrome revision knee system SMITH & NEPHEW, INC. K060742 05/03/2006
crosslinked polyethylene articular inserts SMITH & NEPHEW, INC. K071071 09/19/2007
genesis ii total knee system, legion revision knee system, journey bcs knee system SMITH & NEPHEW, INC. K071790 08/17/2007
legion stem with holes SMITH & NEPHEW, INC. K072531 12/06/2007
tc-plus primary knee system SMITH & NEPHEW, INC. K072858 11/20/2007
smith & nephew, inc. patient matched technology SMITH & NEPHEW, INC. K082358 11/25/2008
journey bcs knee system SMITH & NEPHEW, INC. K091014 09/29/2009
verilast wear claims for the legion primary knee system SMITH & NEPHEW, INC. K093746 04/14/2010
journey cr knee system SMITH & NEPHEW, INC. K101499 08/26/2010
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