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MITEK GII ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K953877
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1995
Days to Decision
165 days
Submission Type
Summary

MITEK GII ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K953877
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1995
Days to Decision
165 days
Submission Type
Summary