K251940
- 510(k) number
- K251940
- Device name
- PathLoc Lumbar Plate System
- Applicant
- L&K BIOMED Co., Ltd. KR
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2026-03-03
- Date received
- 2025-06-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K251940.pdf
Official FDA record: K251940
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.