Clinical results with ProDisc: European experience and U.S. Investigation Device Exemption study

Spine

Volumn 28, Issue 20 SUPPL., 2003, Pages

  Zigler, Jack E ^a  

^a TEXAS BACK INSTITUTE   (United States)

Author keywords

Artificial disc; Lumbar spine; Spinal arthroplasty

Indexed keywords

ADULT; ANTERIOR SPINE FUSION; ARTHROPLASTY; BLEEDING; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; EUROPE; FEMALE; FOLLOW UP; FOOD AND DRUG ADMINISTRATION; HUMAN; LENGTH OF STAY; LUMBAR SPINE; MALE; OPERATION DURATION; PAIN ASSESSMENT; PATIENT SATISFACTION; PRIORITY JOURNAL; PROSTHESIS; QUESTIONNAIRE; RANDOMIZED CONTROLLED TRIAL; REVIEW; UNITED STATES; VISUAL ANALOG SCALE;

EID: 0142121540     PISSN: 03622436     EISSN: None     Source Type: Journal    
DOI: 10.1097/00007632-200310151-00009     Document Type: Review

References (3)

1. Marnay T. Lumbar disc replacement: 7 to 11-year results with Prodisc. Spine J 2002;2:94S.
2. Mayer HM, Wiechert K, Korge A, et al. Minimally invasive total disc replacement: surgical technique and preliminary clinical results. Eur Spine J 2002;11(suppl 2):S124-S130.
3. Bertagnoli R, Kumar S. Indications for full prosthetic disc arthroplasty: a correlation of clinical outcome against a variety of indications. Eur Spine 2002;11(suppl 2):S131-S136.