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QUICKANCHOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K921873
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1992
Days to Decision
62 days
Submission Type
Summary

QUICKANCHOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K921873
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1992
Days to Decision
62 days
Submission Type
Summary