FDA 510(k) Applications Submitted by Smith & Nephew, Inc

FDA 510(k) Number Submission Date Device Name Applicant
K170282 01/30/2017 Smith & Nephew VISIONAIRE Adaptive Guides Smith & Nephew, Inc
K082211 08/06/2008 RENASYS-F NEGATIVE PRESSURE WOUND THERAPY FOAM DRESSING KITS Smith & Nephew, Inc
K142520 09/08/2014 Smith & Nephew, Inc. Spatialframe.com V5.0 Web-based software Smith & Nephew, Inc
K103793 12/27/2010 DURAFIBER AG Smith & Nephew, Inc
K140879 04/07/2014 BIOSURE HEALICOIL PK INTERFERENCE SCREW Smith & Nephew, Inc
K142948 10/10/2014 BIOSURE REGENESORB interference Screw Smith & Nephew, Inc


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