Medical Device Manufacturer · US , Washington , DC

Artimplant AB - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artimplant AB General & Plastic Surgery ✕

4 devices

1-4 of 4

Cleared Sep 18, 2007

SPORTMESH OR ARTELON TISSUE REINFORCEMENT

General & Plastic Surgery · 71d

Cleared Jan 19, 2006

General & Plastic Surgery · 106d

Cleared Oct 17, 2005

ARTELON SURGICAL SUTURE

General & Plastic Surgery · 38d

Cleared Nov 17, 2003

ARTELON SURGICAL SUTURE

General & Plastic Surgery · 125d