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Vanguard XP Knee System

Page Type
Cleared 510(K)
510(k) Number
K153657
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2016
Days to Decision
141 days
Submission Type
Summary

Vanguard XP Knee System

Page Type
Cleared 510(K)
510(k) Number
K153657
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2016
Days to Decision
141 days
Submission Type
Summary