K090401Substantially Equivalent
Orthoss
Ed. Geistlich Soehne AG Fur Chemische Industrie, Washington DC / Traditional, Substantially Equivalent
K090401 is the FDA 510(k) clearance record for ORTHOSS, a class II device, cleared for Ed. Geistlich Soehne AG Fur Chemische Industrie on under FDA product code MQV (Filler, Bone Void, Calcium Compound). FDA records list 2 510(k) clearances for Ed. Geistlich Soehne AG Fur Chemische Industrie, from to . As of , FDA records show no recalls naming K090401.
Clearance record
- Decision date
- Received
- (325 days to decision)
- Product code
- MQV Filler, Bone Void, Calcium Compound
- Regulation
- 21 CFR 888.3045
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Ed. Geistlich Soehne AG Fur Chemische Industrie 1300 I St., NW, 11th Floor, Washington DC
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code MQV
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
