Sequoia® 3306-5550

GUDID 00889024334977

ZIMMER SPINE, INC.

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00889024334977
NIH Device Record Key8a8a5512-29c7-44fe-980d-81cc27f54f51
Commercial Distribution StatusIn Commercial Distribution
Brand NameSequoia®
Version Model Number3306-5550
Catalog Number3306-5550
Company DUNS787663400
Company NameZIMMER SPINE, 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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter
Length50 Millimeter
Outer Diameter5.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024334977 [Primary]

FDA Product Code

MNIORTHOSIS, SPINAL PEDICLE FIXATION

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


[00889024334977]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-06-23
Device Publish Date2015-09-24

On-Brand Devices [Sequoia®]

008890243353633313-080
008890243353493313-070
008890243353323313-065
008890243353253313-060
008890243353183313-055
008890243353013313-050
008890243352953313-045
008890243352883313-040
008890243352573311-510
008890243355543384-3
008890243355473373-1
008890243355303372-1
008890243355233367-2
008890243355163363-1
008890243355093361-075
008890243354933361-065
008890243354863361-055
008890243354793361-045
008890243354623360-075
008890243354553360-065
008890243354483360-055
008890243354313360-045
008890243354243360-040
008890243354173356-2
008890243354003313-100
008890243353943313-095
008890243353873313-090
008890243353703313-085
008890243353563313-075
008890243352713313-035
008890243352643313-030
008890243352333310-50
008890243352263309-40
008890243352193308-35
008890243352023306-8560
008890243351963306-8555
008890243351893306-8550
008890243351723306-8545
008890243351653306-8540
008890243351583306-8535
008890243351413306-8530
008890243351343306-7560
008890243351273306-7555
008890243351103306-7550
008890243351033306-7545
008890243350973306-7540
008890243350803306-7535
008890243350733306-7530
008890243350663306-6560
008890243350593306-6555

Trademark Results [Sequoia]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SEQUOIA
SEQUOIA
98386839 not registered Live/Pending
Elijah Storm Cramer
2024-02-01
SEQUOIA
SEQUOIA
98377926 not registered Live/Pending
Sequoia Consulting Group, LLC
2024-01-26
SEQUOIA
SEQUOIA
98322126 not registered Live/Pending
Sequoia Capital Operations, LLC
2023-12-19
SEQUOIA
SEQUOIA
98133023 not registered Live/Pending
American Cast Iron Pipe Company
2023-08-15
SEQUOIA
SEQUOIA
98107435 not registered Live/Pending
First American Financial Corporation
2023-07-28
SEQUOIA
SEQUOIA
97774365 not registered Live/Pending
Preeminence LLC
2023-01-31
SEQUOIA
SEQUOIA
97704013 not registered Live/Pending
Sequoia Capital Operations, LLC
2022-12-05
SEQUOIA
SEQUOIA
97700510 not registered Live/Pending
AMERICAN HDD, LLC
2022-12-01
SEQUOIA
SEQUOIA
97635561 not registered Live/Pending
USmills LLC
2022-10-17
SEQUOIA
SEQUOIA
97629939 not registered Live/Pending
Unison Hardware, Inc.
2022-10-12
SEQUOIA
SEQUOIA
97549428 not registered Live/Pending
Sequoia Medical Practice PLLC
2022-08-15
SEQUOIA
SEQUOIA
97240441 not registered Live/Pending
LABELIUM SAS
2022-01-26

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