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BIOKNOTLESS ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K002639
510(k) Type
Traditional
Applicant
MITEK PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2001
Days to Decision
260 days
Submission Type
Summary

BIOKNOTLESS ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K002639
510(k) Type
Traditional
Applicant
MITEK PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2001
Days to Decision
260 days
Submission Type
Summary