![From QSR to QMSR: Meeting FDA’s New Requirements From QSR to QMSR: Meeting FDA’s New Requirements](https://www.fdanews.com/ext/resources/Book-Covers-NEW/From-QSR-to-QMSR-500.png?height=200&t=1714569011&width=200)
Home » ChoiceSpine Granted FDA Clearance Hawkeye Ti
ChoiceSpine Granted FDA Clearance Hawkeye Ti
October 6, 2017
ChoiceSpine received 510(k) clearance from the FDA to market Hawkeye Ti, a 3D printed titanium vertebral body replacement device.
The device offers the same implant portfolio as the original Peek Hawkeye device with the added advantage of a 3D printed, open titanium structure optimized for bone in-growth. Hawkeye Ti is the first 3D printed devices being developed and commercialized by ChoiceSpine.
The Hawkeye was designed to stabilize and fuse the vertebral column with simple implants in a variety of shapes and sizes.
Upcoming Events
-
21Oct