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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