Raymedica, Inc. Receives FDA Approval To Initiate Patient Enrollment In The HydraFlex(TM) Nucleus Arthroplasty System(TM) Clinical Trial

MINNEAPOLIS--(BUSINESS WIRE)--June 29, 2006--Raymedica today announced that it has received FDA approval to begin enrolling patients in a US clinical study to evaluate the potential benefits of its HydraFlex(TM) Nucleus Arthroplasty System(TM), a new non-fusion technology for the treatment of degenerative disc disease.

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