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Conformis iTotal Cruciate Retaining (CR) Knee Replacement System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180906
510(k) Type
Special
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2018
Days to Decision
40 days
Submission Type
Summary

Conformis iTotal Cruciate Retaining (CR) Knee Replacement System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180906
510(k) Type
Special
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2018
Days to Decision
40 days
Submission Type
Summary