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Home » Orthopaedic Implant’s Wrist Fracture Device Gains 510(k) Clearance
Orthopaedic Implant’s Wrist Fracture Device Gains 510(k) Clearance
Reno, Nev.-based Orthopaedic Implant has received 510(k) clearance from the FDA for its DRPx wrist fracture plating system.
The titanium implant, which is intended for use in outpatient surgeries, features a low-profile pre-contoured plate and screw design to minimize the impact on soft tissue.
The system also includes variable-angle and fixed-angle locking screws and indicator lines for improved guidance and adjustment, the company said.
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