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MITEK 2GII MENISCAL REPAIR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002406
510(k) Type
Traditional
Applicant
Mitek Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2001
Days to Decision
192 days
Submission Type
Summary

MITEK 2GII MENISCAL REPAIR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002406
510(k) Type
Traditional
Applicant
Mitek Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2001
Days to Decision
192 days
Submission Type
Summary