FDA UDI
In Commercial Distribution
🇺🇸 United States
SpinePlex
DI: 04546540434364
·
Model: 0406202000
·
STRYKER CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- SpinePlex
- Primary DI
- 04546540434364
- Version / Model
- 0406202000
- Catalog Number
- 0406-202-000
- Company Name
- STRYKER CORPORATION
- Labeler DUNS
- 196548481
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-06-30
- Public Version
- 5
- Public Version Date
- 2023-03-02
- Public Version Status
- Update
- Public Device Record Key
- 9151b2c5-cfa4-4696-a497-a833f2fd7f22
Device Description
Radiopaque Bone Cement
Device Characteristics
- Single Use
- Yes
- 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
- 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
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| NDN | CEMENT, BONE, VERTEBROPLASTY | Orthopedic | 888.3027 | 2 |
| LOD | BONE CEMENT | Orthopedic | 888.3027 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 60505 | Vertebral bone filler, non-bioabsorbable | A sterile substance intended to be used to replace cortical/cancellous bone in a vertebral body to stabilize vertebral compression fractures (VCFs) caused by cancer, osteoporosis, or trauma. The device may be a sterile powder of a synthetic polymer [e.g., polymethylmethacrylate (PMMA)] that is mixed with its sterile diluent, or a non-PMMA-containing elastomer formed by mixing two precursors, prior to implantation typically during a balloon kyphoplasty or vertebroplasty procedure. This device does not contain an antibiotic agent. After application, this device cannot be reused. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 34546540434365 | GS1 | pack | 2 | In Commercial Distribution | |
| Primary | 04546540434364 | GS1 | ||||
| Package | 54546540434369 | GS1 | case | 10 | In Commercial Distribution |
Customer Contacts
- Phone
- +1(800)253-3210
- [email protected]