ZIMMER AMBULATORY PUMP PAIN MANAGEMENT SYSTEM

ZIMMER AMBULATORY PUMP PAIN MANAGEMENT SYSTEM is an FDA 510(k)-cleared medical device (K050433) manufactured by Zimmer Orthopaedic Surgical Products. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 12, 2005. Regulation: 8.