Last synced on 25 January 2026 at 3:41 am

KNOTILUS ANCHOR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113297
510(k) Type
Traditional
Applicant
T.A.G. Medical Products Corporation, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2012
Days to Decision
115 days
Submission Type
Summary

KNOTILUS ANCHOR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113297
510(k) Type
Traditional
Applicant
T.A.G. Medical Products Corporation, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2012
Days to Decision
115 days
Submission Type
Summary