Last synced on 10 January 2025 at 11:05 pm

CUPTIMIZE™ Advanced

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231503
510(k) Type
Traditional
Applicant
DePuy Orthopaedics, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2023
Days to Decision
90 days
Submission Type
Summary

CUPTIMIZE™ Advanced

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231503
510(k) Type
Traditional
Applicant
DePuy Orthopaedics, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2023
Days to Decision
90 days
Submission Type
Summary