First Ever Pedicle Screw System with Nanotechnology Designation and Osteoblast and Stem cell data comparing performance to other surface types.
CARMEL, Ind., April 23, 2020 /PRNewswire/ — Nanovis today announced that it received 510(k) clearance for a bioceramic nanotube surface on its Nano FortiFix Pedicle Screw System.
“Surgeons and distributors have been very complementary of the nanotechnology benefits of our Nano FortiCore interbodies and have requested to pair them with nanotechnology enhanced pedicle screws. We plan to offer a complete portfolio of nanotechnology enhanced pedicle screw systems to include open, percutaneous, midline, and deformity, to give patients the most advanced technology possible,” says Nanovis’ VP of Sales, Jeff Shepherd.
Nanovis is an award-winning bio-device technology company committed to helping surgeons, hospitals, and patients achieve excellent fixation and infection outcomes using advanced tech platforms. Its industry-leading fixation technologies offer surgeons and hospitals the best aspects of fixation, visualization, and durability. Nanovis’ developmental infection technology platforms promise to offer surgeons and hospitals much-needed bactericidal solutions.
Nanovis is actively expanding distribution for bioceramic nanotube enhanced Nano FortiFix pedicle screws and bioceramic nanotube enhanced Nano FortiCore interbodies. To discuss opportunities, please contact Jeff Shepherd, Vice President of Sales, at Jeff.Shepherd@NanovisTechnology.com.
Nanovis discovers, develops, and commercializes innovative technology platforms designed for superior fixation and infection outcomes. Nanovis is commercializing the following innovative technology platforms: a bioceramic enhanced nanotube surface, a deeply porous titanium scaffold (licensed from Sites Medical), a pre-clinical bioceramic bactericidal nanotube surface technology, and a pre-clinical localized infection technology potentially capable of killing multi-drug resistant bacteria within minutes.