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RSB Spine's InterPlate™ Vertebral Body Replacement Implant System, Granted Conditional USFDA 510(k) Approval
Filed in archive Diagnostics , Treatment by Gloria Gamat on September 1, 2006
RSB Spine's InterPlate™ Vertebral Body Replacement Implant System, Granted Conditional USFDA 510(k) Approval
A private medical device company focused on developing innovative spinal implants, RSB Spine, LLC has been recently granted conditional approval by the USFDA for the company's 510(k) application that would permit marketing of the InterPlate™ Vertebral Body Replacement System.

Spinal fusion is one of the most common spinal procedures performed by neurosurgeons and orthopedic spine surgeons.

The InterPlate™ Vertebral Body Replacement System is a unique spinal implant designed to rapidly facilitate this process and is used in conjunction with graft material to fuse two or more spinal vertebrae together.

According to Robert S. Bray Jr., M.D., a neurosurgeon who has performed over 7,500 spine surgeries, director of St. Johns Spine Institute in Santa monica, CA, and inventor of the InterPlate™ said:

"The InterPlate™ is a next- generation device incorporating the best features of plate and interbody designs without the drawbacks. I believe its innovative design and unique features will appeal to spine surgeons and that it will soon become the implant of choice for single-level spinal fusion."


RSB Spine, LLC executives are confidents that the InterPlate™ can rapidly become a major revenue generator and change how spinal fusions are viewed, mainly because of the overwhelming positive response from surgeons who have seen the Interplate™.

Source: PR Newswire

Permalink: RSB Spine's InterPlate™ Vertebral Body Replacement Implant System, Granted Conditional USFDA 510(k) Approval
Tags: spinal  implant  interplateâ„¢  spine  system  vertebral+body  body+replacement  interplate&acir 
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