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Zimmer Biomet Universal Navigation System

Page Type
Cleared 510(K)
510(k) Number
K192133
510(k) Type
Traditional
Applicant
Zimmer Biomet Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/2019
Days to Decision
83 days
Submission Type
Summary

Zimmer Biomet Universal Navigation System

Page Type
Cleared 510(K)
510(k) Number
K192133
510(k) Type
Traditional
Applicant
Zimmer Biomet Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/2019
Days to Decision
83 days
Submission Type
Summary