Last synced on 10 January 2025 at 11:05 pm

ARTHROCARE CONTROLLER, MODEL H2000; ARTHROCARE CABLE, MODEL H0970-02; FOOTSWITCH, MODEL H2000-04; POWERCORD, MODEL H2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011634
510(k) Type
Special
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2001
Days to Decision
21 days
Submission Type
Summary

ARTHROCARE CONTROLLER, MODEL H2000; ARTHROCARE CABLE, MODEL H0970-02; FOOTSWITCH, MODEL H2000-04; POWERCORD, MODEL H2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011634
510(k) Type
Special
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2001
Days to Decision
21 days
Submission Type
Summary