K252873
- 510(k) number
- K252873
- Device name
- Q Interbody Instruments
- Applicant
- K2m, Inc. VA · US
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2026-02-06
- Date received
- 2025-09-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K252873.pdf
Official FDA record: K252873
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.