Stryker has launched its ES2 Spinal System to build on its current Xia 3 pedicle screw.
Spinal Tech
U.K.-based Invibio now has 500 PEEK-OPTIMA biomaterial devices cleared for commercial use in the U.S. and more than 80 in China.
San Clemente, Calif.-based VertiFlex plans to sell some of its non-core spine technology to Stryker.
The Food and Drug Administration granted 41 orthopedic- and spine-related device clearances in February.
Stephen Cook, PhD, joined the board of directors of Parsippany, N.J.-based Precision Spine.
Fishers, Ind.-based Nexxt Spine will move its headquarters and manufacturing plan to Noblesville, Ind., according to the Indianapolis Business Journal.
The FDA sent Stryker a warning letter for quality concerns at the device maker's Portage, Mich., facility, according to Medscape Today.
Amedica has named Karl Farnsworth, CPA, chief financial officer. The company has also recently added four executive management officers: Kevin Ontiverso will serve as chief legal and compliance officer, Jim Abraham as senior vice president of sales, Paul Sendro as…
Israel-based NLT Spine has opened a U.S. subsidiary to increase commercialization of its device technology platform.
The FDA granted 510(k) clearance to Alphatec Spine's Alphatec Solus internal fixation anterior lumbar interbody fusion device.
