| Primary Device ID | M7402700011 |
| NIH Device Record Key | 77ebe70c-ba62-4db6-9ef7-daba73336675 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Rampart-O |
| Version Model Number | 83-05-01-11 |
| Catalog Number | 270-0011 |
| Company DUNS | 033014361 |
| Company Name | SPINEOLOGY INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| 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 | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com | |
| Phone | 651-256-8500 |
| info@spineology.com |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Height | 11 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M7402700011 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
[M7402700011]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-10 |
| Device Publish Date | 2024-05-31 |
| M7402700013 | Distractor Paddle, 13 mm |
| M7402700012 | Distractor Paddle, 12 mm |
| M7402700011 | Distractor Paddle, 11 mm |
| M7402700010 | Distractor Paddle, 10 mm |
| M7402700009 | Distractor Paddle, 9 mm |
| M7402700008 | Distractor Paddle, 8 mm |
| M7402700007 | Distractor Paddle, 7 mm |
| M7402700016 | Distractor Paddle, 16 mm |
| M7402700015 | Distractor Paddle, 15 mm |
| M7402700014 | Distractor Paddle, 14 mm |
| M7402500041 | Rampart Remover |
| M7402700021 | Slap Mallet Extension |