Responsive Arthroscopy, LLC
Responsive Arthroscopy Suture Anchor System
SKU K202153UPC MBI
In Stock
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IIFDA 510(k) Cleared (K202153)
1
Free shipping on orders over $99 · 30-day returns
Responsive Arthroscopy, LLC
Free shipping on orders over $99 · 30-day returns
Responsive Arthroscopy Suture Anchor System is an FDA 510(k)-cleared medical device (K202153) 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 September 8, 2020. Regulation: 8.
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