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FDA 510(k)

MAVERICK External Fixation System

K-Number: K213874 · 2022-02-11

ApplicantSmith & Nephew, Inc.
Decision Date2022-02-11
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MAVERICK External Fixation System is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-02-11 under approval number K213874. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAVERICK External Fixation System?

MAVERICK External Fixation System is a medical device that received FDA 510(k) clearance on 2022-02-11. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K213874.

When was MAVERICK External Fixation System approved by the FDA?

MAVERICK External Fixation System received FDA 510(k) clearance on 2022-02-11, under approval number K213874.

What company makes MAVERICK External Fixation System?

MAVERICK External Fixation System is manufactured by Smith & Nephew, Inc..

What is the FDA product code for MAVERICK External Fixation System?

The FDA product code for MAVERICK External Fixation System is JDW.

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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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