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 |
| K240113 |
01/16/2024 |
CORIOGRAPH Knee Pre-Op Plan |
Smith & Nephew, Inc |
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