Last synced on 13 June 2025 at 11:06 pm

LnK Posterior Cervical Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143278
510(k) Type
Traditional
Applicant
L&K BIOMED Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/29/2015
Days to Decision
257 days
Submission Type
Summary

LnK Posterior Cervical Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143278
510(k) Type
Traditional
Applicant
L&K BIOMED Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/29/2015
Days to Decision
257 days
Submission Type
Summary