Last synced on 25 January 2026 at 3:41 am

RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023667
510(k) Type
Special
Applicant
Plus Orthopedics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2002
Days to Decision
54 days
Submission Type
Summary

RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023667
510(k) Type
Special
Applicant
Plus Orthopedics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2002
Days to Decision
54 days
Submission Type
Summary