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ARTiC-L 3D Ti Spinal System with TiONIC Technology, ARTiC-XL 3D Ti Spinal System with TiONIC Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190959
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2019
Days to Decision
82 days
Submission Type
Summary

ARTiC-L 3D Ti Spinal System with TiONIC Technology, ARTiC-XL 3D Ti Spinal System with TiONIC Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190959
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2019
Days to Decision
82 days
Submission Type
Summary