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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)
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)
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