Last synced on 14 November 2025 at 11:06 pm

MAXIM ACCEL KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023546
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2003
Days to Decision
87 days
Submission Type
Summary

MAXIM ACCEL KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023546
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2003
Days to Decision
87 days
Submission Type
Summary