| Primary Device ID | 10705034014654 |
| NIH Device Record Key | 820acde7-3100-434d-8e9b-5f62bce45b4c |
| Commercial Distribution Discontinuation | 2019-11-30 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DOC |
| Version Model Number | 73100165 |
| Catalog Number | 73100165 |
| Company DUNS | 107105876 |
| Company Name | DEPUY SPINE, 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10705034014654 [Primary] |
| KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10705034014654]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-11-07 |
| Device Publish Date | 2015-09-24 |
| 10705034014678 | DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS LOCKING PLATFORM |
| 10705034014661 | DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS NONLOCKING PLATFORM |
| 10705034014654 | DOC VENTRAL CERVICAL STABILIZATION SYSTEM DIVERGENT PLATFORM LOCKING |
| 10705034014647 | DOC VENTRAL CERVICAL STABILIZATION SYSTEM DIVERGENT PLATFORM NONLOCKING |