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PATIENT MATCHED TITANIUM ALLOY TROCHLEA

Page Type
Cleared 510(K)
510(k) Number
K001350
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2000
Days to Decision
89 days
Submission Type
Summary

PATIENT MATCHED TITANIUM ALLOY TROCHLEA

Page Type
Cleared 510(K)
510(k) Number
K001350
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2000
Days to Decision
89 days
Submission Type
Summary