SpineJack 0909-100-042
GUDID 03760253800518
PREPARATION KIT 4.2MM
STRYKER CORPORATION
Orthopaedic prosthesis implantation instrument, single-use| Primary Device ID | 03760253800518 |
| NIH Device Record Key | 46847f27-2e3e-4d32-bfe2-d31dba8eabec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SpineJack |
| Version Model Number | 0909100042 |
| Catalog Number | 0909-100-042 |
| Company DUNS | 196548481 |
| Company Name | STRYKER CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 03760253800518 [Primary] |
FDA Product Code
| HXG | TAMP |
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 | 2020-08-04 |
| Device Publish Date | 2020-07-27 |
On-Brand Devices [SpineJack]
| 33760253800564 | CEMENT PUSHER 4.2MM |
| 33760253800557 | CEMENT PUSHER 5.0-5.8MM |
| 33760253800540 | INJECTOR TRANSFER TUBE 4.2MM |
| 33760253800533 | INJECTOR TRANSFER TUBE 5.0-5.8MM |
| 03760253800525 | PREPARATION KIT 5.8MM |
| 03760253800518 | PREPARATION KIT 4.2MM |
| 03760253800501 | PREPARATION KIT 5.0MM |
Trademark Results [SpineJack]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SPINEJACK 77148228 3539345 Live/Registered |
Vexim, SAS 2007-04-04 |
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