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FDA 510(k)

Admiral ACP System

K-Number: K212139 · 2021-09-01

ApplicantSeaSpine Orthopedics Corporation
Decision Date2021-09-01
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Admiral ACP System is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2021-09-01 under approval number K212139. 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 Admiral ACP System?

Admiral ACP System is a medical device that received FDA 510(k) clearance on 2021-09-01. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K212139.

When was Admiral ACP System approved by the FDA?

Admiral ACP System received FDA 510(k) clearance on 2021-09-01, under approval number K212139.

What company makes Admiral ACP System?

Admiral ACP System is manufactured by SeaSpine Orthopedics Corporation.

What is the FDA product code for Admiral ACP System?

The FDA product code for Admiral ACP System is 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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