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FDA 510(k)

Resorbable Mesh Device

K-Number: K172130 · 2017-11-16

ApplicantSeaSpine Orthopedics Corporation
Decision Date2017-11-16
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Resorbable Mesh Device is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2017-11-16 under approval number K172130. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Resorbable Mesh Device?

Resorbable Mesh Device is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K172130.

When was Resorbable Mesh Device approved by the FDA?

Resorbable Mesh Device received FDA 510(k) clearance on 2017-11-16, under approval number K172130.

What company makes Resorbable Mesh Device?

Resorbable Mesh Device is manufactured by SeaSpine Orthopedics Corporation.

What is the FDA product code for Resorbable Mesh Device?

The FDA product code for Resorbable Mesh Device is MQV.

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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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