FDA Registration Active 🇫🇷 France

U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-TRAY114)

Reg #: 3003526896 · FEI: 3003526896 · Expires 2025
Products
4
Proprietary Names
8
Establishment Types
1
Classifications
4

Registration Details

Registration Name
SPINEVISION SAS
Registration Number
3003526896
FEI Number
3003526896
Status
Active
Expiry Year
2025
Initial Importer
No
Address
3 Rue De La Renaissance
City
Antony Hauts-de-Seine
Country
FR

Regulatory Submissions

510(k) Number
K160124

Owner / Operator

Firm Name
SPINEVISION SAS
Operator Number
9048013
Address
3 rue de la Renaissance
City
Antony
State
Paris
Postal Code
F-92160
Country
FR
Correspondent
Quang TRAN

Products

Device Name Product Code
Appliance, Fixation, Spinal Interlaminal KWP
Orthosis, Spinal Pedicle Fixation MNI
Orthosis, Spondylolisthesis Spinal Fixation MNH
Appliance, Fixation, Spinal Intervertebral Body KWQ

Proprietary Names

U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-TRAY114) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-A316) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (SD-RACK1) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-A317) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-TRAY115) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-TRAY112) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-TRAY111) U.L.I.S.™ and LUMIS™ Pedicle Screw Fixation System (IS1-ID)

Establishment Types

Manufacture Medical Device