OZARK Cervical Plate System; PYRENEES® Cervical Plate System; EVEREST® Spinal System; MESA® Spinal System; MESA® Small Stature Spinal System; CASPIAN® Spinal System; DENALI® Spinal System; DENALI® MI Spinal System; YUKON OCT Spinal System; Xia® 3 Spinal System; K2M Patient Specific; CASCADIA™ Interbody System; CAYMAN® Plate System; CAYMAN® Plate System-MI

K242361 is the FDA 510(k) clearance record for OZARK Cervical Plate System; PYRENEES® Cervical Plate System; EVEREST® Spinal System; MESA® Spinal System; MESA® Small Stature Spinal System; CASPIAN® Spinal System; DENALI® Spinal System; DENALI® MI Spinal System; YUKON OCT Spinal System; Xia® 3 Spinal System; K2M Patient Specific; CASCADIA™ Interbody System; CAYMAN® Plate System; CAYMAN® Plate System-MI, a class II device, cleared for Stryker Spine on 2024-11-07 under FDA product code KWQ (Appliance, Fixation, Spinal Intervertebral Body). FDA records list 377 510(k) clearances for HOWMEDICA OSTEONICS CORP, from 1999-01-28 to 2026-07-17. As of 2026-09-10, FDA records show no recalls naming K242361.