Primary Device ID | 10889981115401 |
NIH Device Record Key | efa5a642-ad1a-44d5-819a-fb8795717ad3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cordant |
Version Model Number | 26-07-0477 |
Catalog Number | 26-07-0477 |
Company DUNS | 079840876 |
Company Name | SEASPINE ORTHOPEDICS CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com | |
Phone | +1(760)727-8399 |
custsvcspine@seaspine.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10889981115401 [Primary] |
KWQ | Appliance, fixation, spinal intervertebral body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
[10889981115401]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-04-18 |
10889981137090 | Lid |
10889981137083 | 4 Level Plate Caddy |
10889981137076 | 3 Level Plate caddy |
10889981137069 | 1 & 2 Level Plate caddy |
10889981137052 | Screw Caddy |
10889981137045 | Implant Tray |
10889981137038 | Instrument Tray |
10889981137021 | Base |
10889981121433 | Case |
10889981115623 | Drill - 16mm (07-6007) |
10889981115616 | Drill - 14mm (07-6006) |
10889981115609 | Drill - 12mm (07-6005) |
10889981115593 | Plate Sizing Guide (07-7000) |
10889981115586 | Plate Bender (07-6700) |
10889981115579 | Tap (07-6600) |
10889981115562 | Double Barrel Limited Angle Drill Guide |
10889981115555 | Double Barrel Drill Guide (07-6500) |
10889981115548 | Single Barrel Limited Angle Drill Guide |
10889981115531 | Single Barrel Drill Guide (07-6400) |
10889981115524 | Spring Loaded Awl |
10889981115517 | Awl (07-6300) |
10889981115500 | AO Drill Driver (07-6200) |
10889981115494 | Screwdriver - NonTapered Split Tipped StarDrive |
10889981115487 | Screwdriver - Non-Tapered StarDrive |
10889981115470 | Screwdriver - StarDrive (07-6100) |
10889981115463 | Plate Holder (07-6012) |
10889981115456 | Temporary Fixation Pin (07-6004) |
10889981115449 | 93mm |
10889981115432 | 89mm |
10889981115425 | 85mm |
10889981115418 | 81mm |
10889981115401 | 77mm |
10889981115395 | 73mm |
10889981115388 | 69mm |
10889981115371 | 78mm |
10889981115364 | 75mm |
10889981115357 | 72mm |
10889981115340 | 69mm |
10889981115333 | 66mm |
10889981115326 | 63mm |
10889981115319 | Plate - 3 Level - 60mm (07-0360) |
10889981115302 | 57mm |
10889981115296 | 54mm |
10889981115289 | 55mm |
10889981115272 | 52mm |
10889981115265 | 49mm |
10889981115258 | 46mm |
10889981115241 | 43mm |
10889981115234 | 40mm |
10889981115227 | 37mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CORDANT 97770076 not registered Live/Pending |
Baker Hughes Holdings LLC 2023-01-26 |
CORDANT 86618576 5120231 Live/Registered |
Tyler David Wine Works, LLC 2015-05-04 |
CORDANT 77399040 not registered Dead/Abandoned |
Innovative Spinal Technologies, Inc. 2008-02-16 |
CORDANT 77295942 not registered Dead/Abandoned |
Innovative Spinal Technologies, Inc. 2007-10-04 |
CORDANT 76242878 not registered Dead/Abandoned |
Cordant, Inc. 2001-04-19 |
CORDANT 75444958 not registered Dead/Abandoned |
Thiokol Corporation 1998-03-05 |
CORDANT 75152987 2081575 Dead/Cancelled |
Cordant, Inc. 1996-08-15 |
CORDANT 75152977 2081574 Dead/Cancelled |
Cordant, Inc. 1996-08-15 |
CORDANT 75152976 2083937 Dead/Cancelled |
Cordant, Inc. 1996-08-15 |
CORDANT 75152975 2091136 Dead/Cancelled |
Cordant, Inc. 1996-08-15 |
CORDANT 75152974 2085869 Dead/Cancelled |
Cordant, Inc. 1996-08-15 |
CORDANT 74802126 not registered Dead/Abandoned |
Cordant, Inc. 1993-11-10 |