Brickyard 1020-3224
by Altus Spine
Brickyard 1020-3224 is a Class I device made by Altus Spine, cleared under FDA 510(k) K182406 on 22 Feb 2019 and listed in FDA GUDID since 30 Aug 2024 (UDI-DI 00843210187051), 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 | Number00843210187051 | Date30 Aug 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK182406 | Date22 Feb 2019 | StatusActive |
Official records
- AccessGUDID record 00843210187051
- FDA 510(k) database K182406
Across registries
- FDA 510(k) K182406 decided 22 Feb 2019 Active
- FDA GUDID UDI-DI 00843210187051 listed 30 Aug 2024 Listed
Timeline
- Cleared FDA 510(k) K182406
- Listed FDA GUDID 00843210187051
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Brickyard
- Generic name
- Orthopaedic surgical procedure kit, non-medicated, reusable
- Model / reference
- 1020-3224
- Primary DI / UDI-DI
- 00843210187051
- 510(k) Number
- FDA product code
- LRP
- GMDN term
- Orthopaedic surgical procedure kit, non-medicated, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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