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FDA 510(k)

Stryker Pediatric Mandibular Distractor 2

K-Number: K181504 · 2018-09-11

ApplicantStryker
Decision Date2018-09-11
Product CodeMQN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Stryker Pediatric Mandibular Distractor 2 is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2018-09-11 under approval number K181504. The device is classified under product code MQN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker Pediatric Mandibular Distractor 2?

Stryker Pediatric Mandibular Distractor 2 is a medical device that received FDA 510(k) clearance on 2018-09-11. It is manufactured by Stryker. The 510(k) number is K181504.

When was Stryker Pediatric Mandibular Distractor 2 approved by the FDA?

Stryker Pediatric Mandibular Distractor 2 received FDA 510(k) clearance on 2018-09-11, under approval number K181504.

What company makes Stryker Pediatric Mandibular Distractor 2?

Stryker Pediatric Mandibular Distractor 2 is manufactured by Stryker.

What is the FDA product code for Stryker Pediatric Mandibular Distractor 2?

The FDA product code for Stryker Pediatric Mandibular Distractor 2 is MQN.

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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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