FDA UDI
In Commercial Distribution
🇺🇸 United States
Medyssey Poseidon OCT Spinal Fixation System
DI: 08800048403403
·
Model: LPPS3554
·
Medyssey Co., Ltd.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Medyssey Poseidon OCT Spinal Fixation System
- Primary DI
- 08800048403403
- Version / Model
- LPPS3554
- Company Name
- Medyssey Co., Ltd.
- Labeler DUNS
- 688211503
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-04-04
- Public Version
- 1
- Public Version Date
- 2019-04-12
- Public Version Status
- New
- Public Device Record Key
- b872c5f9-d8a7-40cd-a2d8-5555728a26a6
Device Description
Poseidon Smooth Shank Poly-Axial Screw, 3.5X54mm, 4.0mm rod
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- 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 |
|---|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 888.3050 | 2 |
| NKG | Orthosis, Cervical Pedicle Screw Spinal Fixation | Orthopedic | 888.3075 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 57806 | Vertebral body prosthesis, non-sterile | A non-sterile implantable device designed to replace or repair (fuse) the spinal bony segments, or vertebrae, lost or injured as a consequence of, e.g., trauma, deformity, tumour, or degenerative disease. It is typically intended to be used with supplemental spinal fixation and may be used with a bone graft. It is usually made of metal, polymer, or a combination of these materials. This device must be sterilized prior to use. | No | Obsolete |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 08800048403403 | GS1 |