NexGen® Legacy® 00-5961-018-81

GUDID 00889024209695

Zimmer, Inc.

Knee femur prosthesis trial
Primary Device ID00889024209695
NIH Device Record Keya2e306b0-63b8-4674-aa5c-495219e91c67
Commercial Distribution StatusIn Commercial Distribution
Brand NameNexGen® Legacy®
Version Model Number00-5961-018-81
Catalog Number00-5961-018-81
Company DUNS056038268
Company NameZimmer, 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@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

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
GS100889024209695 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MBHPROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

[00889024209695]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2020-05-11
Device Publish Date2016-05-24

On-Brand Devices [NexGen® Legacy®]

008890245641145996-17-92
008890245641075996-17-91
008890245640915990-17-92
008890245640845990-17-91
008890245640535990-16-02
008890245640465990-16-01
008890245640395990-15-02
008890245640225990-15-01
008890245640155990-14-02
008890245640085990-14-01
008890245639955990-13-02
008890245639885990-13-01
008890245639715990-12-02
008890245639645990-12-01
008890242246505992-17-92
008890242269515996-18-17
008890242269445996-18-14
008890242269375996-18-12
008890242269205996-18-10
008890242268765996-17-17
008890242268695996-17-14
008890242268525996-17-12
008890242268455996-17-10
008890242268145996-16-17
008890242268075996-16-14
008890242267915996-16-12
008890242267845996-16-10
008890242267395996-15-17
008890242267225996-15-14
008890242267155996-15-12
008890242267085996-15-10
008890242265555996-08-17
008890242265485996-08-14
008890242265315996-08-12
008890242265245996-08-10
008890242265175996-07-17
008890242265005996-07-14
008890242264945996-07-12
008890242264875996-07-10
008890242264705996-06-17
008890242264635996-06-14
008890242264565996-06-12
008890242264495996-06-10
008890242264325996-05-17
008890242264255996-05-14
008890242264185996-05-12
008890242264015996-05-10
008890242263955996-04-17
008890242263885996-04-14
008890242263715996-04-12

Trademark Results [NexGen]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NEXGEN
NEXGEN
98867523 not registered Live/Pending
Pro-Line Industrial Products, Inc.
2024-11-22
NEXGEN
NEXGEN
98488003 not registered Live/Pending
NEXGEN INNOVATION LIMITED
2024-04-08
NEXGEN
NEXGEN
98151874 not registered Live/Pending
NexGen Surveying
2023-08-25
NEXGEN
NEXGEN
98124323 not registered Live/Pending
Cascade Corporation
2023-08-09
NEXGEN
NEXGEN
98073423 not registered Live/Pending
ChlorKing, Inc.
2023-07-06
NEXGEN
NEXGEN
97821507 not registered Live/Pending
Nexgen Global, LLC
2023-03-03
NEXGEN
NEXGEN
97821460 not registered Live/Pending
Nexgen Global, LLC
2023-03-03
NEXGEN
NEXGEN
97814118 not registered Live/Pending
Josh Trujillo
2023-02-27
NEXGEN
NEXGEN
97662703 not registered Live/Pending
Addison HVAC LLC
2022-11-04
NEXGEN
NEXGEN
97662699 not registered Live/Pending
Addison HVAC LLC
2022-11-04
NEXGEN
NEXGEN
97390401 not registered Live/Pending
Easy Automation, Inc.
2022-04-30
NEXGEN
NEXGEN
97390400 not registered Live/Pending
Easy Automation, Inc.
2022-04-30
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.