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

Lignende værker

• 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
  af: Holt, Richard T., et al.
  Udgivet: (2007)
• Analysis of adjacent segment reoperation after lumbar total disc replacement
  af: Rainey, Scott, et al.
  Udgivet: (2012)
• The importance of the anterior longitudinal ligament in lumbar disc arthroplasty: 36-Month follow-up experience in extreme lateral total disc replacement
  af: Marchi, Luis, et al.
  Udgivet: (2012)
• 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
  af: Geisler, Fred H., et al.
  Udgivet: (2009)
• Lumbar Disc Replacement for Junctional Decompensation After Fusion Surgery: Clinical and Radiological Outcome at an Average Follow-Up of 33 Months
  af: Hähnle, Ulrich R., et al.
  Udgivet: (2007)