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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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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