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MITEK GIII ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931782
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/22/1994
Days to Decision
469 days
Submission Type
Statement

MITEK GIII ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931782
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/22/1994
Days to Decision
469 days
Submission Type
Statement