ORTHOLOC 3DI PLATING SYSTEM

GUDID 00889797067218

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic fixation plate, non-bioabsorbable, non-sterile
Primary Device ID00889797067218
NIH Device Record Key7945ff22-ff36-4e6a-814f-ea3ec6d575e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameORTHOLOC 3DI PLATING SYSTEM
Version Model Number58889001
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889797067218 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPlate, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889797067218]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-02-19
Device Publish Date2017-12-14

On-Brand Devices [ORTHOLOC 3DI PLATING SYSTEM]

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