Cyclops Anterior Cervical Plate System
K-Number: K213901 · 2022-01-07
Device Summary
Frequently Asked Questions
What is the Cyclops Anterior Cervical Plate System?
Cyclops Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2022-01-07. It is manufactured by Degen Medical. The 510(k) number is K213901.
When was Cyclops Anterior Cervical Plate System approved by the FDA?
Cyclops Anterior Cervical Plate System received FDA 510(k) clearance on 2022-01-07, under approval number K213901.
What company makes Cyclops Anterior Cervical Plate System?
Cyclops Anterior Cervical Plate System is manufactured by Degen Medical.
What is the FDA product code for Cyclops Anterior Cervical Plate System?
The FDA product code for Cyclops Anterior Cervical Plate System is KWQ.
Related Clinical Trials
Other Devices by Degen Medical
Related Devices (Code: KWQ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.