Stryker Craniomaxillofacial

Stryker Craniomaxillofacial holds 3 FDA 510(k) medical device clearances, first cleared 2007, most recent 2024.

Top product codes for Stryker Craniomaxillofacial

JEY — Dental2 devices
HBE — Neurology1 device

Recent clearances by Stryker Craniomaxillofacial

K232350 — Stryker Facial iD SystemCode JEY·2024-01-13
K092743 — THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEMCode JEY·2010-01-15
K070876 — STRYKER TWIST DRILLSCode HBE·2007-04-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.