Providence Medical’s Recent FDA 510(k) Clearances

Providence Medical Technology received FDA 510(k) clearance for ALLY™ Facet Screws and for standalone use of the CAVUX™ Cervical Cage-L System. The clearances complement the DTRAX® Spinal System.

Titanium-based CAVUX Cervical Cage-L offers proprietary grit-blasted and acid-etched surfaces, a large space for allogenic and autogenous bone graft and includes self-drilling and self-tapping screws for additional standalone fixation.

Also titanium based, ALLY Facet Screws provide temporary stabilization as an adjunct to spinal fusion.

In 4Q16, the company closed a $10.5MM new equity financing round to support commercialization and expansion of its cervical fusion products.

Sources: Providence Medical Technology, Inc.; ORTHOWORLD Inc.