K262639
- 510(k) number
- K262639
- Device name
- BAGUERA® C Cervical Disc Surgical Instruments
- Applicant
- Spineart SA CH
- Product code
- QLQ — Manual Instruments Designed For Use With Total Disc
- Decision date
- 2026-08-14
- Date received
- 2026-07-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K262639.pdf
Official FDA record: K262639
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.