Last synced on 25 January 2026 at 3:41 am

ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, SPINE WANDS, ORTHOWANDS, ARTHROWANDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992581
510(k) Type
Traditional
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
129 days
Submission Type
Summary

ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, SPINE WANDS, ORTHOWANDS, ARTHROWANDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992581
510(k) Type
Traditional
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
129 days
Submission Type
Summary