K260546
- 510(k) number
- K260546
- Device name
- Q Pedicle Instruments
- Applicant
- K2m, Inc. VA · US
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2026-03-17
- Date received
- 2026-02-18
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K260546.pdf
Official FDA record: K260546
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.