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KNOTILUS ANCHOR SYSTEM

Page Type
Cleared 510(K)
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)
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