Last synced on 23 May 2025 at 11:06 pm

LnK Cervical Interbody Fusion Cage System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151677
510(k) Type
Special
Applicant
L&K BIOMED Co.,Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/15/2015
Days to Decision
23 days
Submission Type
Summary

LnK Cervical Interbody Fusion Cage System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151677
510(k) Type
Special
Applicant
L&K BIOMED Co.,Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/15/2015
Days to Decision
23 days
Submission Type
Summary