Company ยท US
Artimplant AB
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2007. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 18, 2007 | K071887 | SPORTMESH OR ARTELON TISSUE REINFORCEMENT Artimplant AB | FTL |
| Jun 7, 2007 | K061956 | ARTELON STT SPACER Artimplant AB | KYI |
| Jun 1, 2007 | K061954 | ARTELON CMC SPACER ARTHRO Artimplant AB | KYI |
| Jan 19, 2006 | K052830 | SPORTMESH Artimplant AB | FTL |
| Oct 17, 2005 | K052482 | ARTELON SURGICAL SUTURE Artimplant AB | GAR |
| Sep 21, 2004 | K040070 | ARTELON SPACER CMC-1 Artimplant AB | KYI |
| Nov 17, 2003 | K032160 | ARTELON SURGICAL SUTURE Artimplant AB | GAR |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||