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Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical Interbody Fusion System, InFix Anterior Lumbar System, TraXis Vertebral Body Replacement (Ti and VUE)

Page Type
Cleared 510(K)
510(k) Number
K143297
510(k) Type
Traditional
Applicant
Zimmer Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/2015
Days to Decision
87 days
Submission Type
Summary

Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical Interbody Fusion System, InFix Anterior Lumbar System, TraXis Vertebral Body Replacement (Ti and VUE)

Page Type
Cleared 510(K)
510(k) Number
K143297
510(k) Type
Traditional
Applicant
Zimmer Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/2015
Days to Decision
87 days
Submission Type
Summary