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SPINEVISION LUMIS CANNULATED PEDICLE SCREW FIXATION SYSTEM, SPINEVISION 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
K133575
510(k) Type
Traditional
Applicant
SPINEVISION, S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/30/2014
Days to Decision
222 days
Submission Type
Summary

SPINEVISION LUMIS CANNULATED PEDICLE SCREW FIXATION SYSTEM, SPINEVISION 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
K133575
510(k) Type
Traditional
Applicant
SPINEVISION, S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/30/2014
Days to Decision
222 days
Submission Type
Summary