CoLink™ View
GUDID 00817906021462
Y-Plate Compression Insert, Ti
IN2BONES USA, LLC
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile| Primary Device ID | 00817906021462 |
| NIH Device Record Key | 158c353f-cafb-4fbc-aaf2-127d9c7e0af6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CoLink™ View |
| Version Model Number | P40 ST634 |
| 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 | false |
| 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 | +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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817906021462 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K172300
FDA Product Code
| HRS | Plate, Fixation, Bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-10 |
| Device Publish Date | 2018-08-10 |
On-Brand Devices [CoLink™ View]
| 00817906024197 | Lapidus Transverse Insert, L, PEEK |
| 00817906024180 | Lapidus Transverse Insert, R, PEEK |
| 00817906024173 | Y-Plate Transverse Insert, PEEK |
| 00817906024166 | MTP Transverse Insert, PEEK |
| 00817906021462 | Y-Plate Compression Insert, Ti |
| 00817906021455 | Lapidus/MTP Compression Insert , Ti |
| 00817906021448 | Y-Plate Transverse Insert, Ti |
| 00817906021431 | Lapidus Transverse Insert, L, Ti |
| 00817906021424 | Lapidus Transverse Insert, R, Ti |
| 00817906021417 | MTP Transverse Insert, Ti |
| 00817906020397 | Y-Plate, 5-Hole with Peek Insert |
| 00817906020380 | Lapidus Plate,+2 mm with PEEK Insert, Left |
| 00817906020373 | Lapidus Plate,+2 mm with PEEK Insert, Right |
| 00817906020366 | Lapidus Plate,+1 mm with PEEK Insert, Left |
| 00817906020359 | Lapidus Plate,+1 mm with PEEK Insert, Right |
| 00817906020342 | Lapidus Plate, Std. with PEEK Insert, Left |
| 00817906020335 | Lapidus Plate, Std. with PEEK Insert, Right |
| 00817906020304 | MTP Plate, 6-Hole with PEEK Insert, Left |
| 00817906020298 | MTP Plate, 6-Hole with PEEK Insert, Right |
| 00817906020281 | MTP Plate, 5-Hole with PEEK Insert, Left |
| 00817906020274 | MTP Plate, 5-Hole with PEEK Insert, Right |
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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