Cove Putty, OsteoCove Putty

Cove Putty, OsteoCove Putty is an FDA 510(k)-cleared medical device (K242273) manufactured by SeaSpine Orthopedics Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 24, 2024. Regulation: 8.