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MITEK MINI ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936311
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/31/1995
Days to Decision
559 days
Submission Type
Statement

MITEK MINI ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936311
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/31/1995
Days to Decision
559 days
Submission Type
Statement