Last synced on 14 November 2025 at 11:06 pm

AGC AND MAXIM KNEE COMPONENTS WITH NTS

Page Type
Cleared 510(K)
510(k) Number
K922285
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1992
Days to Decision
90 days
Submission Type
Summary

AGC AND MAXIM KNEE COMPONENTS WITH NTS

Page Type
Cleared 510(K)
510(k) Number
K922285
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1992
Days to Decision
90 days
Submission Type
Summary