Orthopedic Designs North America (ODi-NA) received FDA 510(k) clearance for the Talon® DistalFix® Humeral Nail, a cannulated design available in multiple diameters and lengths. The device is indicated for humeral shaft fractures and is intended to eliminate the need for freehand drilling and distal locking screws.
Talon DistalFix technology, which first received FDA clearance in 2011, has been implanted in >5,000 procedures. ODi-NA’s portfolio includes the DistalFix Femoral Nail and the Talon Compression Hip Screw, as well as a 7.0mm cannulated screw to treat High femoral neck fractures.
Source: Orthopedic Designs North America
Orthopedic Designs North America (ODi-NA) received FDA 510(k) clearance for the Talon® DistalFix® Humeral Nail, a cannulated design available in multiple diameters and lengths. The device is indicated for humeral shaft fractures and is intended to eliminate the need for freehand drilling and distal locking screws. ...
Orthopedic Designs North America (ODi-NA) received FDA 510(k) clearance for the Talon® DistalFix® Humeral Nail, a cannulated design available in multiple diameters and lengths. The device is indicated for humeral shaft fractures and is intended to eliminate the need for freehand drilling and distal locking screws.
Talon DistalFix technology, which first received FDA clearance in 2011, has been implanted in >5,000 procedures. ODi-NA’s portfolio includes the DistalFix Femoral Nail and the Talon Compression Hip Screw, as well as a 7.0mm cannulated screw to treat High femoral neck fractures.
Source: Orthopedic Designs North America
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