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VANGUARD 360 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K093293
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2010
Days to Decision
366 days
Submission Type
Summary

VANGUARD 360 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K093293
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2010
Days to Decision
366 days
Submission Type
Summary