Last synced on 14 November 2025 at 11:06 pm

MG II TOTAL KNEE SYSTEM STEMMED TIBIAL BASEPLATE COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K050723
510(k) Type
Special
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2005
Days to Decision
30 days
Submission Type
Summary

MG II TOTAL KNEE SYSTEM STEMMED TIBIAL BASEPLATE COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K050723
510(k) Type
Special
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2005
Days to Decision
30 days
Submission Type
Summary