Artimplant AB
Artimplant AB appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 18, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K071887 | SPORTMESH OR ARTELON TISSUE REINFORCEMENT | September 18, 2007 |
| K061956 | ARTELON STT SPACER | June 7, 2007 |
| K061954 | ARTELON CMC SPACER ARTHRO | June 1, 2007 |
| K052830 | SPORTMESH | January 19, 2006 |
| K052482 | ARTELON SURGICAL SUTURE | October 17, 2005 |
| K040070 | ARTELON SPACER CMC-1 | September 21, 2004 |
| K032160 | ARTELON SURGICAL SUTURE | November 17, 2003 |