Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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