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Cardima Inc.

Latest From Cardima Inc.

FzioMed Oxiplex Dispute Panel Postponed So CDRH Can Review More Data

With more data submitted to CDRH, FzioMed and the device center have agreed to postpone a planned June 10 dispute-resolution panel meeting on the firm’s previously rejected PMA for the Oxiplex spine surgery gel.

Medical Device Regulation

Regulatory Roundup: FDA Panels; Proteomics; Experiential Learning; 510(k)s

FDA has officially scheduled the first meeting of its Medical Devices Dispute Resolution Panel in more than seven years to assess the case of FzioMed Inc.’s PMA for the Oxiplex gel for lumbar spine surgery. An ophthalmic devices panel has been set for a new corneal implant, and more regulatory news.

Medical Device Regulation

FzioMed Gets Second Chance For Oxiplex Gel PMA With Dispute Resolution Panel

FDA granted FzioMed’s petition for an independent review of its Oxiplex gel PMA by the Medical Devices Dispute Resolution Panel in response to FzioMed’s November 2012 petition. The agency deemed the device, intended for use in spine surgery, as “not approvable” in 2008.

Medical Device Regulation

Device PIPEs Flush with Opportunity

A review of private investments in publicly traded medical device companies in 2008.
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Company Information

  • Industry
  • Medical Devices
    • Implantable Devices
    • Radiofrequency Devices
    • Surgical Equipment & Devices
      • Minimally or Less Invasive
  • Therapeutic Areas
  • Cardiovascular
  • Alias(es)
  • Ownership
  • Headquarters
  • Worldwide
    • North America
      • USA
  • Parent & Subsidiaries
  • Cardima Inc.
  • Senior Management
  • Robert Cheney, CEO
    Ronald E Bourquin, CFO
    Sung Chun, MD, CMO
  • Contact Info
  • Cardima Inc.
    Phone: (510) 354-0300
    47266 Benicia St.
    Fremont, CA 94538