00-5842-021-08

GUDID 00889024633520

Zimmer, Inc.

Unicondylar knee insert
Primary Device ID00889024633520
NIH Device Record Keydabcac25-730c-47bf-b4c2-d2a7bb8bb0a6
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5842-21-08
Catalog Number00-5842-021-08
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
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

Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0
Height8 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024633520 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSXPROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-07
Device Publish Date2022-02-25

Devices Manufactured by Zimmer, Inc.

00889024665927 - NexGen® Complete Knee Solution2024-08-01
00889024673939 - Modified PSN Fem 4-in-1 Cut Block SZ 32024-07-29
00889024673946 - Modified PSN Fem 4-in-1 Cut Block SZ 42024-07-29
00889024673953 - Modified PSN Fem 4-in-1 Cut Block SZ 52024-07-29
00889024673960 - Modified PSN Fem 4-in-1 Cut Block SZ 62024-07-29
00889024673977 - Modified PSN Fem 4-in-1 Cut Block SZ 72024-07-29
00889024673984 - Modified PSN Fem 4-in-1 Cut Block SZ 82024-07-29
00889024673991 - Modified PSN Fem 4-in-1 Cut Block SZ 92024-07-29

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