Arthrosurface, Inc.
Patello-Femoral Wave (Kahuna) Arthroplasty System
SKU K181280UPC KRR
In Stock
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IIFDA 510(k) Cleared (K181280)
1
Free shipping on orders over $99 · 30-day returns
Arthrosurface, Inc.
Free shipping on orders over $99 · 30-day returns
Patello-Femoral Wave (Kahuna) Arthroplasty System is an FDA 510(k)-cleared medical device (K181280) manufactured by Arthrosurface, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 13, 2018. Regulation: 8.
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