ArthroCare Corporation
ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND
SKU K132099UPC GEI
In Stock
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IIFDA 510(k) Cleared (K132099)
1
Free shipping on orders over $99 · 30-day returns
ArthroCare Corporation
Free shipping on orders over $99 · 30-day returns
ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND is an FDA 510(k)-cleared medical device (K132099) manufactured by ArthroCare Corporation. 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 August 21, 2013. Regulation: 8.
