Last synced on 18 April 2025 at 11:05 pm

Tibial baseplate, Tibial insert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222700
510(k) Type
Special
Applicant
United Orthopedic Corporation
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/6/2022
Days to Decision
29 days
Submission Type
Summary

Tibial baseplate, Tibial insert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222700
510(k) Type
Special
Applicant
United Orthopedic Corporation
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/6/2022
Days to Decision
29 days
Submission Type
Summary