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MITEK ANCHOR, MITEK ANCHOR II

Page Type
Cleared 510(K)
510(k) Number
K920213
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1992
Days to Decision
106 days
Submission Type
Statement

MITEK ANCHOR, MITEK ANCHOR II

Page Type
Cleared 510(K)
510(k) Number
K920213
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1992
Days to Decision
106 days
Submission Type
Statement