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Tyber Medical receives CE Mark approval for TyPEEK interbody fusion device

Tyber Medical, a developer of spine and orthopaedic devices, has received CE Mark approval for its TyPEEK, a titanium plasma sprayed PEEK interbody system.

The highly differentiated proprietary titanium plasma sprayed TyPEEK offers benefits of bone growth with titanium along with the modulus and the post op imaging characteristics of PEEK.

The TyPEEK interbody fusion devices include configurations for anterior cervical, anterior lumbar, posterior lumbar, oblique lumbar, transforaminal lumbar, and direct lateral interbody spacers, and are designed for situations where PEEK alone may not provide the best setting for fusion.

Tyber Medical CEO Jeff Tyber noted the Tyber Medical Interbody portfolio offers the company’s customers immediate access to a regulatory approved system, ranging from economical non-sterile PEEK to its highly differentiated proprietary titanium plasma sprayed TyPEEK.

"We are excited to give the versatility and customization of choice back to our customer, with the option to purchase a full system solution or an al la cart selection; trays, instrument, or implant," Tyber added.