Osteo AG
Osteo AG appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 30, 1994.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K933340 | OSTEO INTERLOCKING-COMPRESSION NAIL | June 30, 1994 |
| K922194 | OSTEO STEINMANN PIN | July 23, 1992 |
| K922196 | OSTEO TIBIA NAIL | July 23, 1992 |
| K922195 | OSTEO FEMORAL NAIL | July 23, 1992 |
| K922193 | OSTEO KIRSCHNER WIRE | July 23, 1992 |
| K920149 | OSTEO EX-FI-RE | April 9, 1992 |
| K920037 | OSTEO COMPRESSION HIP SCREW | March 11, 1992 |
| K914374 | OSTEO CERCLAGE WIRE | December 30, 1991 |
| K913559 | OSTEO COMPLETE PNEUMATIC DRILL-OSCILAIR | November 7, 1991 |