MAGEC® Wand MML-001

GUDID 00812258026899

Magnet locator - for use with the MAGEC® Spinal Bracing and Distraction System

NUVASIVE SPECIALIZED ORTHOPEDICS, INC.

Trans-facet-screw internal spinal fixation system, sterile Trans-facet-screw internal spinal fixation system, sterile Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use
Primary Device ID00812258026899
NIH Device Record Key81907428-d4ca-4508-8c68-78f4d6148b86
Commercial Distribution StatusIn Commercial Distribution
Brand NameMAGEC® Wand
Version Model NumberMML-001
Catalog NumberMML-001
Company DUNS837845234
Company NameNUVASIVE SPECIALIZED ORTHOPEDICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone855-435-5477
Emailcsdepartment@ellipse-tech.com
Phone855-435-5477
Emailcsdepartment@ellipse-tech.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com
Phone855-435-5477
Emailcsdepartment@nuvasive.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100812258026899 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument
PGNGrowing Rod System- Magnetic Actuation

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-04-25
Device Publish Date2015-12-23

On-Brand Devices [MAGEC® Wand]

00812258026899Magnet locator - for use with the MAGEC® Spinal Bracing and Distraction System
00812258022259Magnet locator - for use with the MAGEC® Spinal Bracing and Distraction System

Trademark Results [MAGEC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MAGEC
MAGEC
86711404 not registered Dead/Abandoned
NUVASIVE, INC.
2015-07-31
MAGEC
MAGEC
77886556 4411323 Live/Registered
NUVASIVE, INC.
2009-12-04
MAGEC
MAGEC
73408690 1270642 Dead/Cancelled
Al Lee & Associates, Inc.
1983-01-10

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