Cordant 26-07-0354

GUDID 10889981115296

54mm

SEASPINE ORTHOPEDICS CORPORATION

Spinal fixation plate, non-bioabsorbable
Primary Device ID10889981115296
NIH Device Record Keyd3061fb2-de95-4231-87ee-78d231ee0807
Commercial Distribution StatusIn Commercial Distribution
Brand NameCordant
Version Model Number26-07-0354
Catalog Number26-07-0354
Company DUNS079840876
Company NameSEASPINE ORTHOPEDICS CORPORATION
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(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.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 Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110889981115296 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAppliance, fixation, spinal intervertebral body

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


[10889981115296]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-04-18

On-Brand Devices [Cordant]

10889981137090Lid
108899811370834 Level Plate Caddy
108899811370763 Level Plate caddy
108899811370691 & 2 Level Plate caddy
10889981137052Screw Caddy
10889981137045Implant Tray
10889981137038Instrument Tray
10889981137021Base
10889981121433Case
10889981115623Drill - 16mm (07-6007)
10889981115616Drill - 14mm (07-6006)
10889981115609Drill - 12mm (07-6005)
10889981115593Plate Sizing Guide (07-7000)
10889981115586Plate Bender (07-6700)
10889981115579Tap (07-6600)
10889981115562Double Barrel Limited Angle Drill Guide
10889981115555Double Barrel Drill Guide (07-6500)
10889981115548Single Barrel Limited Angle Drill Guide
10889981115531Single Barrel Drill Guide (07-6400)
10889981115524Spring Loaded Awl
10889981115517Awl (07-6300)
10889981115500AO Drill Driver (07-6200)
10889981115494Screwdriver - NonTapered Split Tipped StarDrive
10889981115487Screwdriver - Non-Tapered StarDrive
10889981115470Screwdriver - StarDrive (07-6100)
10889981115463Plate Holder (07-6012)
10889981115456Temporary Fixation Pin (07-6004)
1088998111544993mm
1088998111543289mm
1088998111542585mm
1088998111541881mm
1088998111540177mm
1088998111539573mm
1088998111538869mm
1088998111537178mm
1088998111536475mm
1088998111535772mm
1088998111534069mm
1088998111533366mm
1088998111532663mm
10889981115319Plate - 3 Level - 60mm (07-0360)
1088998111530257mm
1088998111529654mm
1088998111528955mm
1088998111527252mm
1088998111526549mm
1088998111525846mm
1088998111524143mm
1088998111523440mm
1088998111522737mm

Trademark Results [Cordant]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CORDANT
CORDANT
97770076 not registered Live/Pending
Baker Hughes Holdings LLC
2023-01-26
CORDANT
CORDANT
86618576 5120231 Live/Registered
Tyler David Wine Works, LLC
2015-05-04
CORDANT
CORDANT
77399040 not registered Dead/Abandoned
Innovative Spinal Technologies, Inc.
2008-02-16
CORDANT
CORDANT
77295942 not registered Dead/Abandoned
Innovative Spinal Technologies, Inc.
2007-10-04
CORDANT
CORDANT
76242878 not registered Dead/Abandoned
Cordant, Inc.
2001-04-19
CORDANT
CORDANT
75444958 not registered Dead/Abandoned
Thiokol Corporation
1998-03-05
CORDANT
CORDANT
75152987 2081575 Dead/Cancelled
Cordant, Inc.
1996-08-15
CORDANT
CORDANT
75152977 2081574 Dead/Cancelled
Cordant, Inc.
1996-08-15
CORDANT
CORDANT
75152976 2083937 Dead/Cancelled
Cordant, Inc.
1996-08-15
CORDANT
CORDANT
75152975 2091136 Dead/Cancelled
Cordant, Inc.
1996-08-15
CORDANT
CORDANT
75152974 2085869 Dead/Cancelled
Cordant, Inc.
1996-08-15
CORDANT
CORDANT
74802126 not registered Dead/Abandoned
Cordant, Inc.
1993-11-10

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