Copeland Shoulder, Biomet - ShoulderDoc.co.uk

References1Williams GR, Iannotti JP: “Anatomy and biomechanics of the glenohumeral joint related to shoulder arthroplasty.” Seminars in Arthroplasty 11(1):2-15, 2000.2Boileau P, Walch G: “Three-dimensional geometry of the proximal humerus: Implications for surgical technique and prosthetic design.” J Bone Joint Surg (B) 1997; 79-B: 857-65.3Levy O, Bruguera J, Kelly C: Copeland SA: “Cementless surface replacement arthroplasty of the shoulder — 11 years experience.” ICCS, Sydney, 1998.4Levy O, Copeland SA: “Cementless surface replacement arthroplasty of the shoulder: 5 to 10 year results with the Copeland, Mark-2 prostheses.” J Bone Joint Surg (B), 2000; 83-B: 213-21.5Mackenzie DB: “The antero-superior exposure for total shoulder replacement.” Orthop. Traumatol 1993; 2:71-7.This brochure describes the surgical technique used by Steven A. Copeland, F.R.C.S. Biomet, as the manufacturer of this device, does not practice medicine and does not recommend this or anyother surgical technique for use on a specific patient. The surgeon who performs any implant procedure is responsible for determining and using the appropriate techniques for implanting theprosthesis in each individual patient. Biomet is not responsible for selection of the appropriate surgical technique to be used for an individual patient.The Copeland Surface Replacement Arthroplasty (CSRA) of the shoulder was developed by Steven A. Copeland, F.R.C.S., Consultant Orthopaedic Surgeon at the RoyalBerkshire Hospital, Reading, England, U.K.This device is intended to be used in the United States as described in the product labeling.Copeland and MacroBond ® are trademarks of Biomet, Inc.8