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ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000); ARTHROCARE PATIENT CABLE; FOOT CONTROL; POWER CORD; WANDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030551
510(k) Type
Special
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2003
Days to Decision
14 days
Submission Type
Summary

ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000); ARTHROCARE PATIENT CABLE; FOOT CONTROL; POWER CORD; WANDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030551
510(k) Type
Special
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2003
Days to Decision
14 days
Submission Type
Summary