K241117
- 510(k) number
- K241117
- Device name
- M6-C Single Use, Disposable Instrumentation
- Applicant
- Spinal Kinetics / Orthofix / Seaspine CA · US
- Product code
- QLQ — Manual Instruments Designed For Use With Total Disc
- Decision date
- 2024-06-21
- Date received
- 2024-04-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K241117.pdf
Official FDA record: K241117
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.