510(k) for Interpore's bone plate system:
This article was originally published in Clinica
Interpore Cross International of Irvine, California, has received 510(k) clearance from the FDA for its bone plate system for treating internal fixation of pelvic fractures. The contoured, titanium bone plates are compatible with magnetic resonance imaging and computer tomography procedures and features screw holes which can be spaced intraoperatively to fit the anatomy of the patient. The system also allows bone graft material to be placed after the plate and screws are implanted.