Atlas FDA

PathLoc Lumbar Plate System

FDA 510(k) clearance K251940 · decided 2026-03-03

Clearance details

K-number
K251940
Device name
PathLoc Lumbar Plate System
Applicant
L&K BIOMED Co., Ltd.
Decision
Substantially Equivalent
Date received
2025-06-24
Decision date
2026-03-03
Days to decision
252 days
Clearance type
Traditional
Product code
KWQ
Device class
2
Regulation number
888.3060
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Yongin-Si, KR
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Palisades™ Buttress Plate System (K261309)Bethesda Medical Devices, LLC2026-07-16
ARIES Anterior Cervical Plate Systems (K252776)ZheJiang Decans Medical Devices Co., Ltd.2026-05-14
CastleLoc-P Anterior Cervical Plate System (K261112)L&K BIOMED Co., Ltd.2026-05-06
corra™ cervical plating system (K260570)Carlsmed, Inc.2026-04-22
VyPlate™ Anterior Cervical Plate System (K260697)Vy Spine, LLC2026-03-27
ANTERIS Thoracolumbar Plate System (K260015)SpineCraft2026-03-04
Aster (K254182)Osteonic Co., Ltd.2026-02-26
Lumbar Spine Truss System - Plating Solution (LSTS-PS) (K253201)4Web, Inc.2026-02-12
aprevo® cervical plating system (K252611)Carlsmed, Inc.2025-12-22
Proximity Anterior Cervical Plate System; Segmental Plating System (SPS) (K251965)Alphatec Spine, Inc.2025-08-28
Resolve Anterior Cervical Plate System (K251436)Pioneer Surgical Technology, Inc.2025-07-11
Frida™ Anterior Cervical Plate System (K250446)Spineup, Inc.2025-05-23

Recalls involving this device

No recalls on record reference this clearance.