Mont Blanc Spinal Systems MB1LTH

GUDID 03663422000118

LAMINAR THORACIC HOOK

SPINEWAY

Bone-screw internal spinal fixation system hook
Primary Device ID03663422000118
NIH Device Record Key14b283a3-67a6-48ff-ada3-bf03bc1730c1
Commercial Distribution Discontinuation2026-01-30
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMont Blanc Spinal Systems
Version Model Number1
Catalog NumberMB1LTH
Company DUNS281075270
Company NameSPINEWAY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com
Phone+33472770152
Emailinfo@spineway.com

Device Identifiers

Device Issuing AgencyDevice ID
GS103663422000118 [Primary]

FDA Product Code

OSHPedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2026-02-02
Device Publish Date2016-09-08

On-Brand Devices [Mont Blanc Spinal Systems]

03663422002020TRANSVERSE HOOK
03663422000699PEDICLE HOOK
03663422000118LAMINAR THORACIC HOOK

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