FDA UDI
In Commercial Distribution
🇺🇸 United States
Rampart One Lumbar Interbody Fusion System
DI: M7404902032
·
Model: 49-02-01-32
·
SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Rampart One Lumbar Interbody Fusion System
- Primary DI
- M7404902032
- Version / Model
- 49-02-01-32
- Catalog Number
- 490-2032
- Company Name
- SPINEOLOGY INC.
- Labeler DUNS
- 033014361
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-11-08
- Public Version
- 1
- Public Version Date
- 2019-11-18
- Public Version Status
- New
- Public Device Record Key
- 2cc659f0-3a59-4703-a536-1d98de335cbd
Device Description
Rampart One Trial, 18mm, M, 16°
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Unsafe
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Moist Heat or Steam Sterilization
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| OVD | Intervertebral fusion device with integrated fixation, lumbar | Orthopedic | 888.3080 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 60847 | Polymeric spinal fusion cage, sterile | A sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae, typically due to degenerative intervertebral disks [i.e., degenerative disc disease (DDD)]. The device is typically designed as a small, hollow and/or porous, threaded or fenestrated cylinder (or other geometric form) and is made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for bone fusion to occur. Fixation screws and disposable devices associated with implantation may be included with the device. | No | Obsolete |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | M7404902032 | HIBCC |
Customer Contacts
- Phone
- +1(651)256-8500 ext. 534
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K192047 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Height | 18 | Millimeter | |
| Device Size Text, specify | Medium Footprint | ||
| Device Size Text, specify | 16° Lordosis |