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FDA 510(k)

Anterior Cervical Plate System

K-Number: K151553 · 2016-02-10

ApplicantOsteomed Implantes, Ltda
Decision Date2016-02-10
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Anterior Cervical Plate System is a medical device manufactured by Osteomed Implantes, Ltda. It received FDA 510(k) clearance on 2016-02-10 under approval number K151553. 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 Anterior Cervical Plate System?

Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2016-02-10. It is manufactured by Osteomed Implantes, Ltda. The 510(k) number is K151553.

When was Anterior Cervical Plate System approved by the FDA?

Anterior Cervical Plate System received FDA 510(k) clearance on 2016-02-10, under approval number K151553.

What company makes Anterior Cervical Plate System?

Anterior Cervical Plate System is manufactured by Osteomed Implantes, Ltda.

What is the FDA product code for Anterior Cervical Plate System?

The FDA product code for Anterior Cervical Plate System is KWQ.

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Related Devices (Code: 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.

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