Ebi, L.P.
MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM
SKU K030372UPC KTT
In Stock
—
IIFDA 510(k) Cleared (K030372)
1
Free shipping on orders over $99 · 30-day returns
Ebi, L.P.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM is an FDA 510(k)-cleared medical device (K030372) manufactured by Ebi, L.P.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 5, 2003. Regulation: 8.
