Complications of Lumbar Artificial Disc Replacement Compared to Fusion: Results From the Prospective, Randomized, Multicenter US Food and Drug Administration Investigational Device Exemption Study of the Charité Artificial Disc

Ähnliche Einträge

• Prospective, Randomized, Multicenter FDA IDE Study of CHARITÉ Artificial Disc versus Lumbar Fusion: Effect at 5-year Follow-up of Prior Surgery and Prior Discectomy on Clinical Outcomes Following Lumbar Arthroplasty
  von: Geisler, Fred H., et al.
  Veröffentlicht: (2009)
• The First 18 Months Following Food and Drug Administration Approval of Lumbar Total Disc Replacement in the United States: Reported Adverse Events Outside an Investigational Device Exemption Study Environment
  von: Blumenthal, Scott L., et al.
  Veröffentlicht: (2007)
• Artificial disc: preliminary results of a prospective study in the United States
  von: Hochschuler, Stephen H., et al.
  Veröffentlicht: (2002)
• The Charité III Artificial Disc lumbar disc prosthesis: assessment of medium-term results
  von: Gioia, G., et al.
  Veröffentlicht: (2007)
• Kineflex lumbar artificial disc versus Charité lumbar total disc replacement for the treatment of degenerative disc disease: A randomized non-inferiority trial with minimum of 2 years’ follow-up
  von: Pettine, Kenneth, et al.
  Veröffentlicht: (2011)