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MITEK MINI ANCHOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K930892
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1994
Days to Decision
339 days
Submission Type
Statement

MITEK MINI ANCHOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K930892
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1994
Days to Decision
339 days
Submission Type
Statement