The U.S. Food and Drug Administration (FDA) has granted 510(k) clearance to an expandable lateral lumbar interbody system. Per the 510(k) statement, the device is indicated for “spinal fusion ...
Our opinions are our own. Here is a list of our partners and here's how we make money. Direct Auto Insurance specializes in high-risk drivers, but with a high number of complaints, there may be ...
Objectives Systematic review and meta-analysis of published observational cohort studies. To quantify the increased risk smokers have of experiencing a delayed and/or non-union in fractures, spinal ...