The device has been usesd in more than 15,000 cases globally, according to a news release. It features a wide range of implants for interbody fusion.
Implanet’s CEO, Ludovic Lastennet, said SqualeTM is expected to launch in the U.S. by summer.
Implanet’s SqualeTM anterior cervical cage received FDA 510(k) approval, the devicemaker said April 11.
The device has been usesd in more than 15,000 cases globally, according to a news release. It features a wide range of implants for interbody fusion.
Implanet’s CEO, Ludovic Lastennet, said SqualeTM is expected to launch in the U.S. by summer.