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FDA 510(k)

SeaSpine Cabo ACP (Anterior Cervical Plate) System

K-Number: K173521 · 2018-01-24

ApplicantSeaSpine Orthopedics Corporation
Decision Date2018-01-24
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SeaSpine Cabo ACP (Anterior Cervical Plate) System is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2018-01-24 under approval number K173521. 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 SeaSpine Cabo ACP (Anterior Cervical Plate) System?

SeaSpine Cabo ACP (Anterior Cervical Plate) System is a medical device that received FDA 510(k) clearance on 2018-01-24. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K173521.

When was SeaSpine Cabo ACP (Anterior Cervical Plate) System approved by the FDA?

SeaSpine Cabo ACP (Anterior Cervical Plate) System received FDA 510(k) clearance on 2018-01-24, under approval number K173521.

What company makes SeaSpine Cabo ACP (Anterior Cervical Plate) System?

SeaSpine Cabo ACP (Anterior Cervical Plate) System is manufactured by SeaSpine Orthopedics Corporation.

What is the FDA product code for SeaSpine Cabo ACP (Anterior Cervical Plate) System?

The FDA product code for SeaSpine Cabo ACP (Anterior Cervical Plate) System is KWQ.

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Other Devices by SeaSpine Orthopedics Corporation

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Related Devices (Code: KWQ)

K160982Sphynx™Eden Spine, LLC K162638CETRA Anterior Cervical Plate SystemOrthofix, Inc. K162194MEDICREA INTERNATIONAL Anterior Cervical Locking Plate SystemMedicrea International SA K162211AccuFit Lateral Plate SystemPrecision Spine, Inc. K162250FortiBridge Anterior Cervical Plate SystemNanovis Spine, LLC K162664Pyrenees Cervical Plate SystemK2m, Inc.

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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