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MICROFIX QUICKANCHOR PLUS

Page Type
Cleared 510(K)
510(k) Number
K024115
510(k) Type
Traditional
Applicant
MITEK WORLDWIDE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2003
Days to Decision
90 days
Submission Type
Summary

MICROFIX QUICKANCHOR PLUS

Page Type
Cleared 510(K)
510(k) Number
K024115
510(k) Type
Traditional
Applicant
MITEK WORLDWIDE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2003
Days to Decision
90 days
Submission Type
Summary