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

Page Type
Cleared 510(K)
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)
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