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RSB Spine, LLC, Announces Additional FDA Clearance for the InterPlate® L-Ti

September 13, 2010 By Bio-Medicine.Org

CLEVELAND, Sept. 13 /PRNewswire/ — RSB Spine, LLC, today
announced that the InterPlate® L-Ti has been cleared for an
additional product code (KWQ).  The L-Ti was previously
cleared as an interbody fusion device.

RSB Spine Chief Executive Officer John A. Redmond said: “We are
excited about this new clearance. Because of our Bridging Flush
Fit™ design, we have always been of the opinion that the
InterPlate L-Ti can function as an interbody fusion device and/or
anterior lumbar plate. The new product code also simplifies coding
for surgeons, clarifying reimbursement for this type of zero
profile implant.”

RSB Spine is a privately held medical device company focused on
developing innovative spinal implants with a focus on modular
fusion products. News releases and other information on the company
are available on the Internet at: http://www.rsbspine.com.

‘/>”/>

SOURCE

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