PANALOK WEDGE ABSORABLE SUTURE ANCHOR SYSTEM

PANALOK WEDGE ABSORABLE SUTURE ANCHOR SYSTEM is an FDA 510(k)-cleared medical device (K952687) manufactured by ETHICON, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 5, 1996. Regulation: 8.