Osteoprecision Gd-1015-100
Osteoprecision Gd-1015-100 is a bone graft delivery kit (FDA Class II; FDA product code FMF, Syringe, Piston) made by Micromedics, Inc., cleared under FDA 510(k) K151543 on 7 Jul 2015 and listed in FDA GUDID since 25 Sep 2016 (UDI-DI 00815634020382), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00815634020382 | Date25 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK151543 | Date7 Jul 2015 | StatusActive |
Official records
- AccessGUDID record 00815634020382
- FDA 510(k) database K151543
Across registries
- FDA 510(k) K151543 decided 7 Jul 2015 Active
- FDA GUDID UDI-DI 00815634020382 listed 25 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K151543
- Listed FDA GUDID 00815634020382
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Osteoprecision
- Generic name
- Bone graft delivery kit
- Model / reference
- GD-1015-100
- Primary DI / UDI-DI
- 00815634020382
- 510(k) Number
- FDA product code
- FMF
- GMDN term
- Bone graft delivery kit
- Device class
- Class II
- Regulation number
- 880.5860
- GUDID distribution status
- In Commercial Distribution
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