GUDID 00889024319141

ZIMMER TRABECULAR METAL TECHNOLOGY INC.

Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial
Primary Device ID00889024319141
NIH Device Record Key9be2474e-b79d-432a-a465-3cb96cd585da
Commercial Distribution StatusIn Commercial Distribution
Version Model Number96-151-40142
Company DUNS793120965
Company NameZIMMER TRABECULAR METAL 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter
Device Size Text, specify0
Height14 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024319141 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQPSPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


[00889024319141]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-07
Device Publish Date2016-05-25

Devices Manufactured by ZIMMER TRABECULAR METAL TECHNOLOGY INC.

00889024223790 - TM Ardis®2020-06-23
00889024316515 - Mergence™-S2020-06-23
00889024317239 - Mergence™-S2020-06-23
00889024317307 - Mergence™-S2020-06-23
00889024317383 - Mergence™-S2020-06-23
00889024317970 - Mergence™-S2020-06-23
00889024318045 - Mergence™-S2020-06-23
00889024318076 - Mergence™-S2020-06-23

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