Responsive Arthroscopy, LLC
Responsive Arthroscopy Thunderbolt System
SKU K203121UPC MBI
In Stock
—
IIFDA 510(k) Cleared (K203121)
1
Free shipping on orders over $99 · 30-day returns
Responsive Arthroscopy, LLC
Free shipping on orders over $99 · 30-day returns
Responsive Arthroscopy Thunderbolt System is an FDA 510(k)-cleared medical device (K203121) manufactured by Responsive Arthroscopy, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 2021. Regulation: 8.
Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020
Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057