Cortoss 2110-0008
GUDID 00808232000917
Delivery Gun
Stryker Corporation
Orthopaedic cement dispenser| Primary Device ID | 00808232000917 |
| NIH Device Record Key | ecb922d3-e855-4ae0-9dbe-f3799ece0a5e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cortoss |
| Version Model Number | 2110-0008 |
| Catalog Number | 2110-0008 |
| Company DUNS | 149183167 |
| Company Name | Stryker 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 | 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00808232000917 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K080108
FDA Product Code
| NDN | CEMENT, BONE, VERTEBROPLASTY |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [Cortoss]
| 00808232001372 | Delivery Gun Kit |
| 00808232000979 | Bone Augmentation Material |
| 00808232000962 | Bone Augmentation Material |
| 00808232000917 | Delivery Gun |
| 30808232000949 | Mix Tips, Luer |
Trademark Results [Cortoss]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CORTOSS 77292643 3699532 Live/Registered |
ORTHOVITA, INC. 2007-10-01 |
 CORTOSS 75827120 2646320 Live/Registered |
ORTHOVITA, INC. 1999-10-20 |
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