Q Pedicle Instruments
by K2M, Inc.
510(k) K260546
Q Pedicle Instruments is a Class II device made by K2M, Inc., cleared under FDA 510(k) K260546 on 17 Mar 2026, 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 | NumberK260546 | Date17 Mar 2026 | StatusActive |
Official records
- FDA 510(k) database K260546
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- OLO
- Device class
- Class II
- Regulation
- 21 CFR Part 882.4560
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
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