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Identity Imprint Porous Total Knee Replacement System, Identity Imprint Porous Cruciate Retaining Total Knee Replacement System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223316
510(k) Type
Traditional
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2023
Days to Decision
266 days
Submission Type
Summary

Identity Imprint Porous Total Knee Replacement System, Identity Imprint Porous Cruciate Retaining Total Knee Replacement System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223316
510(k) Type
Traditional
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2023
Days to Decision
266 days
Submission Type
Summary