| Primary Device ID | 00840606186537 |
| NIH Device Record Key | eda8c9a7-670c-46f0-845c-7fd44c97c794 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lucent Lateral |
| Version Model Number | 81260-000 |
| Company DUNS | 610712213 |
| Company Name | SPINAL ELEMENTS, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
|---|---|
| GS1 | 00840606186537 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
[00840606186537]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-05 |
| Device Publish Date | 2025-01-28 |
| 00840606184946 | Probe Lateral Light Cable |
| 00840606184922 | Dimension Light Cable |
| 00840606186537 | 1.5mm x 14.5" Titanium K-Wire Arrow Tip |