Minnesota Medical Development, Inc.
MODIFICATION TO REBOUND HRD
SKU K080393UPC FTL
In Stock
—
IIFDA 510(k) Cleared (K080393)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Minnesota Medical Development, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO REBOUND HRD is an FDA 510(k)-cleared medical device (K080393) manufactured by Minnesota Medical Development, Inc.. 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, 2008. Regulation: 8.
