Last synced on 14 November 2025 at 11:06 pm

PathLoc Lumbar Interbody Fusion Cage System

Page Type
Cleared 510(K)
510(k) Number
K251741
510(k) Type
Special
Applicant
L&K BIOMED Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/8/2025
Days to Decision
32 days
Submission Type
Summary

PathLoc Lumbar Interbody Fusion Cage System

Page Type
Cleared 510(K)
510(k) Number
K251741
510(k) Type
Special
Applicant
L&K BIOMED Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/8/2025
Days to Decision
32 days
Submission Type
Summary