K050468Substantially Equivalent
Triabsorb Composite Screw
Advanced Biomaterials, St. Jeannet, FR / Traditional, Substantially Equivalent
K050468 is the FDA 510(k) clearance record for TRIABSORB COMPOSITE SCREW, a class II device, cleared for Advanced Biomaterials on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 3 510(k) clearances for Advanced Biomaterials, from to . As of , FDA records show no recalls naming K050468.
Clearance record
- Decision date
- Received
- (189 days to decision)
- Product code
- HWC Screw, Fixation, Bone
- Regulation
- 21 CFR 888.3040
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Advanced Biomaterials 265 Rte. De La Baronne, St. Jeannet, FR
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HWC
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 1 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 2 |
| April 2026 | 3 |
| May 2026 | 4 |
| June 2026 | 2 |
| July 2026 | 1 |
| August 2026 | 3 |
| September 2026 | 4 |
| 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.
