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MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000511
510(k) Type
Special
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2000
Days to Decision
26 days
Submission Type
Summary

MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000511
510(k) Type
Special
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2000
Days to Decision
26 days
Submission Type
Summary