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VANGUARD SSK 360 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121149
510(k) Type
Special
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2012
Days to Decision
30 days
Submission Type
Summary

VANGUARD SSK 360 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121149
510(k) Type
Special
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2012
Days to Decision
30 days
Submission Type
Summary