CORETRAK

GUDID 00840420137470

WRIGHT MEDICAL TECHNOLOGY, INC.

External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use
Primary Device ID00840420137470
NIH Device Record Key076a698f-a9f9-4f9a-a57d-26156efba1c3
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORETRAK
Version Model NumberEFSR1001
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
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
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

Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter
Device Size Text, specify0
Width8 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100840420137470 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


[00840420137470]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-01

On-Brand Devices [CORETRAK]

00840420143815EF302580
00840420141248EF301580
00840420140630EFSR1000
00840420137470EFSR1001
00840420129031XPCK1303
00840420129024XPCK1300
00840420129017XPCK1200
00840420129000XPCK1002
00840420128997XPCK1001
00840420127280EFSR1200
00840420127273EFSR1002
00889797046923Hex Driver
00889797054300Steripack

Trademark Results [CORETRAK]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CORETRAK
CORETRAK
77529740 3681152 Live/Registered
Wright Medical Technology, Inc.
2008-07-23
CORETRAK
CORETRAK
76036503 not registered Dead/Abandoned
CAMM, INC
2000-04-27

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