Arthrocare Controller, Authrocare Cable, Foot Control, Power Cord, Wands
510(k) K021519
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK021519 | Date6 Jun 2002 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- GEI
- Device Class
- Class II
- Regulation
- 21 CFR Part 878.4400
- Advisory Committee
- General, Plastic Surgery
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 22 Sep 2026
The Arthrocare Controller is a bipolar, high-frequency RF electrosurgical controller for compatible ArthroCare wands and patient cables. It delivers electrical energy to soft tissue for resection, ablation, and coagulation, and provides hemostasis of blood vessels during arthroscopic and orthopedic procedures.
The system includes the controller, patient cable, foot control, power cord, and wands. The ArthroCare wands are bipolar, single-use devices. The system is intended for use in approved surgical workflows for soft-tissue resection, ablation, coagulation, and hemostasis.
Other devices from ArthroCare Corporation
Questions
AI-generated answers, 22 Sep 2026
What is the ArthroCare Controller used for?
The ArthroCare Controller is a bipolar, high-frequency RF electrosurgical controller designed to deliver electrical energy to soft tissue for resection, ablation, coagulation, and hemostasis during arthroscopic and orthopedic procedures.
What components are included in the ArthroCare system?
The system includes the controller, patient cable, foot control, power cord, and ArthroCare wands. The wands are bipolar, single-use devices specifically designed for use with this controller.
Are the ArthroCare wands reusable or single-use?
The ArthroCare wands are single-use devices and should not be reused. This ensures optimal performance and safety during surgical procedures.
What types of procedures is this system intended for?
The system is intended for use in approved surgical workflows for soft-tissue resection, ablation, coagulation, and hemostasis during arthroscopic and orthopedic procedures.