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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
K200227
01/30/2020
Journey II XR Knee Instrument
Smith & Nephew, Inc
K190253
02/07/2019
EVOS Small Fragment Upper Extremity Plates Line Additions
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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