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PATIENT-SPECIFIC VANGUARD FEMORAL COMPONETS

Page Type
Cleared 510(K)
510(k) Number
K102125
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2011
Days to Decision
209 days
Submission Type
Summary

PATIENT-SPECIFIC VANGUARD FEMORAL COMPONETS

Page Type
Cleared 510(K)
510(k) Number
K102125
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2011
Days to Decision
209 days
Submission Type
Summary