Smith & Nephew
FDA 510(k) medical device clearances.
Name variants for Smith & Nephew
as filed with FDA- Smith & Nephew
- Smith+Nephew
Top product codes for Smith & Nephew
Recent clearances by Smith & Nephew
- K241666 — EVOS Pelvic and Acetabular System
- K240487 — EVOS Patella Plates
- K233730 — Footprint Mini PK, 3.5mm Suture Anchor
- K232457 — Q-FIX ULTRA All-Suture Anchor
- K223762 — Smith & Nephew ACCORD Cable System
- K221929 — Smith+Nephew INTELLIO Tablet
- K203566 — Tablet Application
- K201253 — Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation
- K201349 — Smith+Nephew Arthroscopes
- K201198 — S+N Laparoscopes, 4KO, Autoclavable, S+N Bariactric Laparoscopes, 4KO, Autoclavable
- K192876 — INTELLIO Tablet Application
- K190367 — Smith & Nephew Tablet Application
- K172785 — CONQUEST FN
- K163653 — NOVOS-NAIL Limb Lengthening System (LLS)
- K153606 — LENS Camera Control Unit-WiFi, LENS Camera Unit-Non-WiFi, LENS camera head, Camera Coupler, Tablet Application
- K152686 — CONQUEST FN
- K151118 — Smith and Nephew Legion Hinge Knee System
Data sourced from openFDA. This site is unofficial and independent of the FDA.