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QUICKANCHOR II

Page Type
Cleared 510(K)
510(k) Number
K931253
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1994
Days to Decision
461 days
Submission Type
Statement

QUICKANCHOR II

Page Type
Cleared 510(K)
510(k) Number
K931253
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1994
Days to Decision
461 days
Submission Type
Statement