510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K130302Substantially Equivalent

Spinevision Lumis Cannulated Polyaxial Pedicle Screw Fixation System, Spinevision U.l.i.s. Polyaxial Pedicle Screw Fixat

Spinevision Inc., Antony Cedex, FR / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K130302 is the FDA 510(k) clearance record for SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT, a class II device, cleared for Spinevision S.A. on under FDA product code MNI (Orthosis, Spinal Pedicle Fixation). FDA records list 5 510(k) clearances for Spinevision S.A., from to . As of , FDA records show no recalls naming K130302.

Clearance record

Decision date
Received
(173 days to decision)
Product code
MNI Orthosis, Spinal Pedicle Fixation
Regulation
21 CFR 888.3070
Device class
Class II
Review panel
Orthopedic
Applicant
Spinevision S.A. Antony Parc Ii - 10 Pl. Du General De Gaulle, Antony Cedex, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MNI

Trailing 12 months

FDA records hold no clearances under product code MNI in the trailing twelve months.

FDA records show no clearances under product code MNI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MNI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260