Last synced on 3 April 2026 at 11:13 pm

SECULOK™ Suture Anchor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180759
510(k) Type
Traditional
Applicant
U&I Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/9/2018
Days to Decision
140 days
Submission Type
Summary

SECULOK™ Suture Anchor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180759
510(k) Type
Traditional
Applicant
U&I Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/9/2018
Days to Decision
140 days
Submission Type
Summary