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FDA 510(k)

SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System

K-Number: K220711 · 2022-05-10

ApplicantSeaSpine Orthopedics Corporation
Decision Date2022-05-10
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2022-05-10 under approval number K220711. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System?

SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System is a medical device that received FDA 510(k) clearance on 2022-05-10. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K220711.

When was SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System approved by the FDA?

SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System received FDA 510(k) clearance on 2022-05-10, under approval number K220711.

What company makes SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System?

SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System is manufactured by SeaSpine Orthopedics Corporation.

What is the FDA product code for SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System?

The FDA product code for SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System is MAX.

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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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