CAYMAN® Plate System 1208-41F40S
GUDID 10888857019164
Sacral Plate
K2M, INC.
Spinal fixation plate, non-bioabsorbable| Primary Device ID | 10888857019164 |
| NIH Device Record Key | 4b20d317-44f3-465f-a6d5-0b609e95eea2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CAYMAN® Plate System |
| Version Model Number | 1208-41F40S |
| Catalog Number | 1208-41F40S |
| Company DUNS | 146060863 |
| Company Name | K2M, INC. |
| 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 |
Customer Support Contacts
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(703)777-3155 |
| mzellers@k2m.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com | |
| Phone | +1(571)919-2000 |
| mark.zellers@stryker.com |
Device Dimensions
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10888857019164 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K091253
FDA Product Code
| KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
[10888857019164]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [CAYMAN® Plate System]
| 10888857093522 | Screw |
| 10888857093447 | Screw |
| 10888857093362 | Screw |
| 10888857093287 | Screw |
| 10888857093201 | Screw |
| 10888857020085 | Buttress Plate, Size 30 mm |
| 10888857020054 | Buttress Plate |
| 10888857020047 | Buttress Plate |
| 10888857020030 | Buttress Plate |
| 10888857019577 | Lumbar Plate |
| 10888857019560 | Lumbar Plate |
| 10888857019553 | Lumbar Plate |
| 10888857019546 | Lumbar Plate |
| 10888857019539 | Lumbar Plate |
| 10888857019522 | Lumbar Plate |
| 10888857019515 | Lumbar Plate |
| 10888857019508 | Sacral Plate |
| 10888857019492 | Sacral Plate |
| 10888857019485 | Sacral Plate |
| 10888857019478 | Sacral Plate |
| 10888857019461 | Sacral Plate |
| 10888857019454 | Sacral Plate |
| 10888857019447 | Sacral Plate |
| 10888857019430 | Sacral Plate |
| 10888857019423 | Lumbar Plate |
| 10888857019416 | Thoracolumbar Plate |
| 10888857019409 | Thoracolumbar Plate |
| 10888857019393 | Thoracolumbar Plate |
| 10888857019386 | Thoracolumbar Plate |
| 10888857019379 | Thoracolumbar Plate |
| 10888857019362 | Thoracolumbar Plate |
| 10888857019355 | Thoracolumbar Plate |
| 10888857019348 | Thoracolumbar Plate |
| 10888857019331 | Thoracolumbar Plate |
| 10888857019324 | Thoracolumbar Plate |
| 10888857019317 | Thoracolumbar Plate |
| 10888857019300 | Thoracolumbar Plate |
| 10888857019294 | Thoracolumbar Plate |
| 10888857019287 | Thoracolumbar Plate |
| 10888857019270 | Thoracolumbar Plate |
| 10888857019263 | Thoracolumbar Plate |
| 10888857019256 | Thoracolumbar Plate |
| 10888857019249 | Sacral Plate |
| 10888857019232 | Lumbar Plate |
| 10888857019225 | Thoracolumbar Plate |
| 10888857019218 | Sacral Plate |
| 10888857019201 | Lumbar Plate |
| 10888857019195 | Thoracolumbar Plate |
| 10888857019188 | Sacral Plate |
| 10888857019171 | Lumbar Plate |
Trademark Results [CAYMAN]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CAYMAN 98753035 not registered Live/Pending |
Christopher Joseph Caman 2024-09-16 |
 CAYMAN 98451380 not registered Live/Pending |
ROOKE LLC 2024-03-15 |
 CAYMAN 97605934 not registered Live/Pending |
PMK Mess- und Kommunikationstechnik GmbH 2022-09-25 |
 CAYMAN 90294917 not registered Live/Pending |
Yu Jiangyuan 2020-11-03 |
 CAYMAN 88472075 5949267 Live/Registered |
SpectraLight Technologies, Inc. 2019-06-13 |
 CAYMAN 88336022 not registered Dead/Abandoned |
CARRODRAIN B.V.B.A. 2019-03-12 |
 CAYMAN 87691115 5523185 Live/Registered |
Semillas Papalotla 2017-11-20 |
 CAYMAN 86626261 4971978 Live/Registered |
Burnham Services, Inc. 2015-05-12 |
 CAYMAN 86251774 4761558 Live/Registered |
Jacuzzi Inc. 2014-04-14 |
 CAYMAN 85053700 4283351 Live/Registered |
Semillas Papalotla, S.A. DE C.V. 2010-06-03 |
 CAYMAN 79015404 3602568 Live/Registered |
Dr. Ing. h.c. F. Porsche Aktiengesellschaft 2004-07-08 |
 CAYMAN 78677465 not registered Dead/Abandoned |
Jet Line Products South Jersey, LLC 2005-07-25 |
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