CranioSculpt C-FLOW5CC-CAN
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Unverified
Overview
The CranioSculpt Flow Bone Void Filler is a bioabsorbable, non-antimicrobial synthetic material used for bone reconstruction and repair. It provides osteoconductive bone-tissue scaffolds and sometimes osteovascularization to fill cystic defects, repair fractures, and extend autogenous bone grafts. The device is typically provided as cancellous blocks, chips, or granules of varying sizes, or mouldable/fluid materials.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00813845020344 | Date30 Oct 2015 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- CranioSculpt
- Generic Name
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Model / Ref / Catalog
- C-FLOW5CC-CAN
- Primary DI / UDI-DI
- 00813845020344
- FDA Product Code
- GXP
- GMDN Term
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Device Class
- Class II
- Regulation Number
- 882.5300
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Total Volume — 5 Milliliter
Other devices from Skeletal Kinetics LLC
Properties
Other properties (7)
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No