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SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ...

Page Type
Cleared 510(K)
510(k) Number
K112607
510(k) Type
Traditional
Applicant
SPINEVISION, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2012
Days to Decision
274 days
Submission Type
Summary

SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ...

Page Type
Cleared 510(K)
510(k) Number
K112607
510(k) Type
Traditional
Applicant
SPINEVISION, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2012
Days to Decision
274 days
Submission Type
Summary