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MAXIM REMOVABLE MOLDED POLY TIBIA

Page Type
Cleared 510(K)
510(k) Number
K984623
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1999
Days to Decision
65 days
Submission Type
Summary

MAXIM REMOVABLE MOLDED POLY TIBIA

Page Type
Cleared 510(K)
510(k) Number
K984623
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1999
Days to Decision
65 days
Submission Type
Summary