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CONFORMIS TOTAL KNEE REPIAR SYSTEM (ITOTAL) TIBIAL COMPONENT: 6.0 MM THICKNESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080936
510(k) Type
Traditional
Applicant
CONFORMIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2008
Days to Decision
40 days
Submission Type
Summary

CONFORMIS TOTAL KNEE REPIAR SYSTEM (ITOTAL) TIBIAL COMPONENT: 6.0 MM THICKNESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080936
510(k) Type
Traditional
Applicant
CONFORMIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2008
Days to Decision
40 days
Submission Type
Summary