Zimmer Biomet receives FDA 510(k) clearance of Persona OsseoTi keel tibia
Click Here to Manage Email Alerts
Zimmer Biomet Holdings Inc. has announced FDA 510(k) clearance of its Persona OsseoTi keel tibia for patients undergoing cementless total knee replacement, according to a company press release.
The Persona OsseoTi includes a porous version of the Persona anatomic tibia with porous metal technology for biological fixation, which uses 3D printing and anatomical data, according to the release.
“With an increasing number of surgeons opting for cementless procedures for their patients, we are excited to expand our market-leading Persona knee portfolio with the Persona OsseoTi keel tibia, a versatile and surgeon-centered solution for performing a cementless TKR,” Ivan Tornos, CEO of Zimmer Biomet, said in the release. “Adding the Persona OsseoTi keel tibia to our well-established and clinically proven Persona knee system allows surgeons to better address the needs of their patients with a comprehensive single system solution for a cementless or cemented application,” he added.
Read more about
Click Here to Manage Email Alerts