K243281
- 510(k) number
- K243281
- Device name
- LOCK-IN Spinal Fixation System
- Applicant
- Lock-In USA Corp DE · US
- Product code
- NKB — Thoracolumbosacral Pedicle Screw System
- Decision date
- 2024-12-13
- Date received
- 2024-10-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K243281.pdf
Official FDA record: K243281
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.