SKaffold ReNu SKMA-IM05
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00813845020863 | Date30 Oct 2015 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- SKaffold ReNu
- Generic Name
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Model / Ref / Catalog
- SKMA-IM05
- Primary DI / UDI-DI
- 00813845020863
- FDA Product Code
- MQV
- GMDN Term
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Device Class
- Class II
- Regulation Number
- 888.3045
- 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