Arthrocare Corp.
MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS
SKU K000511UPC GEI
In Stock
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IIFDA 510(k) Cleared (K000511)
1
Free shipping on orders over $99 · 30-day returns
Arthrocare Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS is an FDA 510(k)-cleared medical device (K000511) manufactured by Arthrocare Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 2000. Regulation: 8.
