TRYPTIK2 C-Plate Anterior Cervical Plate System
K-Number: K171797 · 2018-02-26
Device Summary
Frequently Asked Questions
What is the TRYPTIK2 C-Plate Anterior Cervical Plate System?
TRYPTIK2 C-Plate Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2018-02-26. It is manufactured by Spineart. The 510(k) number is K171797.
When was TRYPTIK2 C-Plate Anterior Cervical Plate System approved by the FDA?
TRYPTIK2 C-Plate Anterior Cervical Plate System received FDA 510(k) clearance on 2018-02-26, under approval number K171797.
What company makes TRYPTIK2 C-Plate Anterior Cervical Plate System?
TRYPTIK2 C-Plate Anterior Cervical Plate System is manufactured by Spineart.
What is the FDA product code for TRYPTIK2 C-Plate Anterior Cervical Plate System?
The FDA product code for TRYPTIK2 C-Plate Anterior Cervical Plate System is KWQ.
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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.