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VANGUARD 360 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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