ArthroCare gets FDA nod for vertebroplasty product

AuntMinnie.com staff writers
Dec 27, 2004

Medical device firm ArthroCare of Sunnyvale, CA, has received 510(k) clearance from the Food and Drug Administration for its Parallax Acrylic Resin with Tracers bone cement opacifier.

The product has been cleared for the fixation of pathological fractures of the vertebral body in vertebroplasty or kyphoplasty procedures, ArthroCare said.

By AuntMinnie.com staff writers
December 28, 2004

Copyright © 2004 AuntMinnie.com

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