GAITWAY

GUDID 00840420169341

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID00840420169341
NIH Device Record Keya1ac663a-4c06-48e5-bb9d-548b314b7712
Commercial Distribution StatusIn Commercial Distribution
Brand NameGAITWAY
Version Model NumberGTW-0090
Company DUNS807201207
Company NameWRIGHT MEDICAL TECHNOLOGY, INC.
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100840420169341 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


[00840420169341]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-15

On-Brand Devices [GAITWAY]

0084042017063730-100-02
00840420169365GTW-0115
00840420169358GTW-0100
00840420169341GTW-0090
00840420169334GTW-0075
00840420169327GTW-0065

Trademark Results [GAITWAY]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GAITWAY
GAITWAY
90004257 not registered Live/Pending
Comforcare Franchise Systems, LLC
2020-06-16
GAITWAY
GAITWAY
78517616 3099326 Dead/Cancelled
TALAR-MADE LIMITED
2004-11-16
GAITWAY
GAITWAY
77661702 not registered Dead/Abandoned
NEUROSTREAM TECHNOLOGIES GENERAL PARTNERSHIP
2009-02-02
GAITWAY
GAITWAY
74633641 1944256 Dead/Cancelled
Kistler Instrument Corporation
1995-02-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.