Cleared Special

PathLoc Lumbar Interbody Fusion Cage System

K251741 · L & K Biomed Co., Ltd. · Orthopedic

Jul 2025

Decision

32d

Days

Class 2

Risk

About This 510(k) Submission

K251741 is an FDA 510(k) clearance for the PathLoc Lumbar Interbody Fusion Cage System, a Intervertebral Fusion Device With Bone Graft, Lumbar (Class II — Special Controls, product code MAX), submitted by L & K Biomed Co., Ltd. (Yongin-Si, KR). The FDA issued a Cleared decision on July 8, 2025, 32 days after receiving the submission on June 6, 2025. This device falls under the Orthopedic review panel. Regulated under 21 CFR 888.3080.

Submission Details

510(k) Number	K251741 FDA.gov
FDA Decision	Cleared SESE
Date Received	June 06, 2025
Decision Date	July 08, 2025
Days to Decision	32 days
Submission Type	Special
Review Panel	Orthopedic (OR)
Summary	Summary PDF

Device Classification

Product Code	MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 888.3080
Definition	Intended To Stabilize Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft.