Laurimed Spinal Injection System
510(k) K091818
Laurimed Spinal Injection System is a Class II device made by Laurimed, LLC, cleared under FDA 510(k) K091818 on 23 Sep 2009, 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 | FDA 510(k)SESE | NumberK091818 | Date23 Sep 2009 | StatusActive |
Official records
- FDA 510(k) database K091818
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BSP
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5150
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
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