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FDA 510(k)

TRYPTIK2 C-Plate Anterior Cervical Plate System

K-Number: K171797 · 2018-02-26

ApplicantSpineart
Decision Date2018-02-26
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRYPTIK2 C-Plate Anterior Cervical Plate System is a medical device manufactured by Spineart. It received FDA 510(k) clearance on 2018-02-26 under approval number K171797. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.