SPECTRANETICS LEAD LOCKING DEVICE (LLD) #1, #2, #3 LISTER

SPECTRANETICS LEAD LOCKING DEVICE (LLD) #1, #2, #3 LISTER is an FDA 510(k)-cleared medical device (K990713) manufactured by Spectranetics Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 21, 1999. Regulation: 8.