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MITEK ANCHOR II

Page Type
Cleared 510(K)
510(k) Number
K902751
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1990
Days to Decision
32 days

MITEK ANCHOR II

Page Type
Cleared 510(K)
510(k) Number
K902751
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1990
Days to Decision
32 days