| Primary Device ID | M739CP30020 |
| NIH Device Record Key | e49d1e32-1b9e-4b53-9ab9-cdfec43ac796 |
| Commercial Distribution Discontinuation | 2017-08-11 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | 1-Level Cervical Plates, 20 mm |
| Version Model Number | CP30020 |
| Company DUNS | 836975784 |
| Company Name | CAPTIVA SPINE, 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M739CP30020 [Primary] |
| KWQ | Appliance, Fixation, Spinal Intervertebral Body |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
[M739CP30020]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2023-09-18 |
| Device Publish Date | 2015-10-30 |
| M739CP30020 | 1-Level Cervical Plates, 20 mm |