Kinectiv®

GUDID 00889024137776

Zimmer, Inc.

Uncoated hip femur prosthesis, modular
Primary Device ID00889024137776
NIH Device Record Keyef167d2a-b28d-44cc-bbf4-92353c07c87e
Commercial Distribution StatusIn Commercial Distribution
Brand NameKinectiv®
Version Model Number00-7848-003-01
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@zimmer.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024137776 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPHPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-17

On-Brand Devices [Kinectiv®]

0088902413514700-7805-061-01
0088902413452200-7804-053-01
0088902417318765-7713-022-00
0088902417317065-7713-020-00
0088902417316365-7713-017-00
0088902417315665-7713-016-00
0088902417314965-7713-015-00
0088902417313265-7713-013-00
0088902417312565-7713-012-00
0088902417311865-7713-011-00
0088902417310165-7713-010-00
0088902417309565-7713-009-00
0088902417308865-7713-007-00
0088902417307165-7713-006-00
0088902417306465-7713-005-00
0088902413805600-7848-044-01
0088902413804900-7848-044-00
0088902413803200-7848-043-01
0088902413802500-7848-042-01
0088902413801800-7848-041-01
0088902413800100-7848-034-01
0088902413799800-7848-034-00
0088902413798100-7848-033-01
0088902413797400-7848-033-00
0088902413796700-7848-032-01
0088902413795000-7848-031-01
0088902413794300-7848-030-01
0088902413793600-7848-024-01
0088902413792900-7848-024-00
0088902413791200-7848-023-01
0088902413790500-7848-023-00
0088902413789900-7848-022-01
0088902413788200-7848-022-00
0088902413787500-7848-021-01
0088902413786800-7848-020-01
0088902413785100-7848-014-01
0088902413784400-7848-014-00
0088902413783700-7848-013-01
0088902413782000-7848-013-00
0088902413781300-7848-012-01
0088902413780600-7848-012-00
0088902413779000-7848-011-01
0088902413778300-7848-011-00
0088902413777600-7848-003-01
0088902413776900-7848-003-00
0088902413775200-7848-002-01
0088902413774500-7848-002-00
0088902413517800-7805-064-00
0088902413516100-7805-063-00
0088902413515400-7805-062-00

Trademark Results [Kinectiv]

Mark Image

Registration | Serial
Company
Trademark
Application Date
KINECTIV
KINECTIV
86955980 5915134 Live/Registered
Barrett, David W
2016-03-29
KINECTIV
KINECTIV
77027317 3313301 Live/Registered
ZIMMER, INC.
2006-10-23

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