Medical Device Manufacturer · US , Washington , DC

Artimplant AB - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

Recent clearances: SPORTMESH OR ARTELON TISSUE REINFORCEMENT, ARTELON STT SPACER, ARTELON CMC SPACER ARTHRO

View 7 510(k) Devices ↓
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
K071887 · FTL
General & Plastic Surgery · 71d
Cleared Jan 19, 2006
SPORTMESH
K052830 · FTL
General & Plastic Surgery · 106d
Cleared Oct 17, 2005
ARTELON SURGICAL SUTURE
K052482 · GAR
General & Plastic Surgery · 38d
Cleared Nov 17, 2003
ARTELON SURGICAL SUTURE
K032160 · GAR
General & Plastic Surgery · 125d
Filters
Filter by Specialty
All7 General & Plastic Surgery 4 Orthopedic 3