CoLink™ Plating System
GUDID 00817906020533
Plate/Screw Fixation System
IN2BONES USA, LLC
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile| Primary Device ID | 00817906020533 |
| NIH Device Record Key | b9fb6117-f7a2-489e-8407-9676cc82869b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CoLink™ Plating System |
| Version Model Number | V30 ST216 |
| Company DUNS | 079700711 |
| Company Name | IN2BONES USA, LLC |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | 901.260.7931 |
| info@i2b-usa.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com |
Device Dimensions
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Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817906020533 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K163293
FDA Product Code
| HRS | Plate, Fixation, Bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-06-19 |
On-Brand Devices [CoLink™ Plating System]
| 00817906021288 | CoLink™ View Screw, Ø3.5 x 40mm,Transverse |
| 00817906021271 | CoLink™ View Screw, Ø3.5 x 38mm,Transverse |
| 00817906021264 | CoLink™ View Screw, Ø3.5 x 36mm,Transverse |
| 00817906021257 | CoLink™ View Screw, Ø3.5 x 34mm,Transverse |
| 00817906021240 | CoLink™ View Screw, Ø3.5 x 32mm,Transverse |
| 00817906021233 | CoLink™ View Screw, Ø3.5 x 30mm,Transverse |
| 00817906021226 | CoLink™ View Screw, Ø3.5 x 28mm,Transverse |
| 00817906021219 | CoLink™ View Screw, Ø3.5 x 26mm,Transverse |
| 00817906021202 | CoLink™ View Screw, Ø3.5 x 24mm,Transverse |
| 00817906021196 | CoLink™ View Screw, Ø3.5 x 22mm,Transverse |
| 00817906021189 | CoLink™ View Screw, Ø3.5 x 20mm,Transverse |
| 00817906021172 | CoLink™ View Screw, Ø3.5 x 18mm,Transverse |
| 00817906021165 | Plate/Screw Fixation System |
| 00817906021158 | Plate/Screw Fixation System |
| 00817906021141 | Plate/Screw Fixation System |
| 00817906021134 | Plate/Screw Fixation System |
| 00817906021127 | Plate/Screw Fixation System |
| 00817906021110 | Plate/Screw Fixation System |
| 00817906021103 | Plate/Screw Fixation System |
| 00817906021097 | Plate/Screw Fixation System |
| 00817906021080 | Plate/Screw Fixation System |
| 00817906021073 | Plate/Screw Fixation System |
| 00817906021066 | Plate/Screw Fixation System |
| 00817906021059 | Plate/Screw Fixation System |
| 00817906021042 | Plate/Screw Fixation System |
| 00817906021035 | Plate/Screw Fixation System |
| 00817906021028 | Plate/Screw Fixation System |
| 00817906021011 | Plate/Screw Fixation System |
| 00817906021004 | Plate/Screw Fixation System |
| 00817906020991 | Plate/Screw Fixation System |
| 00817906020984 | Plate/Screw Fixation System |
| 00817906020977 | Plate/Screw Fixation System |
| 00817906020960 | Plate/Screw Fixation System |
| 00817906020953 | Plate/Screw Fixation System |
| 00817906020946 | Plate/Screw Fixation System |
| 00817906020939 | Plate/Screw Fixation System |
| 00817906020922 | Plate/Screw Fixation System |
| 00817906020915 | Plate/Screw Fixation System |
| 00817906020908 | Plate/Screw Fixation System |
| 00817906020892 | Plate/Screw Fixation System |
| 00817906020885 | Plate/Screw Fixation System |
| 00817906020878 | Plate/Screw Fixation System |
| 00817906020861 | Plate/Screw Fixation System |
| 00817906020854 | Plate/Screw Fixation System |
| 00817906020847 | Plate/Screw Fixation System |
| 00817906020830 | Plate/Screw Fixation System |
| 00817906020823 | Plate/Screw Fixation System |
| 00817906020816 | Plate/Screw Fixation System |
| 00817906020809 | Plate/Screw Fixation System |
| 00817906020793 | Plate/Screw Fixation System |
Trademark Results [CoLink]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COLINK 86871790 5297174 Live/Registered |
In2Bones USA, LLC 2016-01-11 |
 COLINK 86141742 4635851 Live/Registered |
Colink Digital Technology Co., Ltd 2013-12-12 |
 COLINK 75453954 2287337 Live/Registered |
CoBank, ACB 1998-03-20 |
 COLINK 75331848 2183998 Dead/Cancelled |
Continental Link, Inc. 1997-07-28 |
 COLINK 74582317 not registered Dead/Abandoned |
Chevron Chemical Company 1994-09-30 |
 COLINK 74217580 not registered Dead/Abandoned |
Chevron Chemical Company 1991-10-28 |
 COLINK 73702298 1501129 Dead/Cancelled |
INLEX, INC. 1987-12-21 |
 COLINK 73702297 not registered Dead/Abandoned |
INLEX, INC. 1987-12-21 |
 COLINK 73702296 1530826 Dead/Cancelled |
INLEX, INC. 1987-12-21 |
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