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LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160124
510(k) Type
Special
Applicant
SpineVision S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/4/2016
Days to Decision
75 days
Submission Type
Summary

LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160124
510(k) Type
Special
Applicant
SpineVision S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/4/2016
Days to Decision
75 days
Submission Type
Summary