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

Monday, September 13, 2010

CLEVELAND -- September 13, 2010 -- 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.


CONTACT:
John A. Redmond
Chief Executive Officer
1.866.241.2104
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