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QUICKANCHOR, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921873
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1992
Days to Decision
62 days
Submission Type
Summary

QUICKANCHOR, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921873
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1992
Days to Decision
62 days
Submission Type
Summary