K251741
- 510(k) number
- K251741
- Device name
- PathLoc Lumbar Interbody Fusion Cage System
- Applicant
- L&K BIOMED Co., Ltd. KR
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2025-07-08
- Date received
- 2025-06-06
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251741.pdf
Official FDA record: K251741
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.