ExsoMed receives FDA 510(k) clearance for cannulated lag screw system

ExsoMed Corporation has announced FDA 510(k) clearance of the NanoPhix cannulated lag screw system for use in common fragment fracture surgeries, such as for avulsion, mallet and condylar fractures, according to a press release.
“Surgeons have shared with us their desire for a lag screw system that actually works,” James Young Kim, chief marketing officer of ExsoMed, said in the release. “Current solutions in the marketplace have fallen short of surgeon demands, specifically from a surgical technique and ease of use perspective. NanoPhix and ExsoMed’s innovative dual

ExsoMed Corporation has announced FDA 510(k) clearance of the NanoPhix cannulated lag screw system for use in common fragment fracture surgeries, such as for avulsion, mallet and condylar fractures, according to a press release.
“Surgeons have shared with us their desire for a lag screw system that actually works,” James Young Kim, chief marketing officer of ExsoMed, said in the release. “Current solutions in the marketplace have fallen short of surgeon demands, specifically from a surgical technique and ease of use perspective. NanoPhix and ExsoMed’s innovative dual