Parallax Ezflow Cement Delivery System
by Arthrocare Corp. United States 510(k)
510(k) K051820 Product code OAR
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK051820 | Date6 Sep 2005 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- OAR
- Device Class
- Class I
- Regulation
- 21 CFR Part 888.4200
- Advisory Committee
- Orthopedic
- FDA Decision
- SESE Substantially Equivalent
Other devices from ArthroCare Corporation
Properties & raw data
Show properties, registry sources and raw records
Sources (1)
- FDA 510(k) K051820