Artimplant AB

7 FDA 510(k) medical device clearances.

Top product codes for Artimplant AB

KYI — Orthopedic 3 devices
FTL — General, Plastic Surgery 2 devices
GAR — General, Plastic Surgery 2 devices

Recent clearances by Artimplant AB

K071887 — SPORTMESH OR ARTELON TISSUE REINFORCEMENT FTL · 2007-09-18
K061956 — ARTELON STT SPACER KYI · 2007-06-07
K061954 — ARTELON CMC SPACER ARTHRO KYI · 2007-06-01
K052830 — SPORTMESH FTL · 2006-01-19
K052482 — ARTELON SURGICAL SUTURE GAR · 2005-10-17
K040070 — ARTELON SPACER CMC-1 KYI · 2004-09-21
K032160 — ARTELON SURGICAL SUTURE GAR · 2003-11-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.