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Virage Navigation System

Page Type
Cleared 510(K)
510(k) Number
K212023
510(k) Type
Traditional
Applicant
Zimmer Biomet Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2021
Days to Decision
59 days
Submission Type
Summary

Virage Navigation System

Page Type
Cleared 510(K)
510(k) Number
K212023
510(k) Type
Traditional
Applicant
Zimmer Biomet Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2021
Days to Decision
59 days
Submission Type
Summary