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FDA 510(k)

SeaSpine Shoreline ACS - Anterior Cervical Standalone System

K-Number: K170569 · 2017-06-15

Decision Date2017-06-15
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SeaSpine Shoreline ACS - Anterior Cervical Standalone System is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2017-06-15 under approval number K170569. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SeaSpine Shoreline ACS - Anterior Cervical Standalone System?

SeaSpine Shoreline ACS - Anterior Cervical Standalone System is a medical device that received FDA 510(k) clearance on 2017-06-15. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K170569.

When was SeaSpine Shoreline ACS - Anterior Cervical Standalone System approved by the FDA?

SeaSpine Shoreline ACS - Anterior Cervical Standalone System received FDA 510(k) clearance on 2017-06-15, under approval number K170569.

What company makes SeaSpine Shoreline ACS - Anterior Cervical Standalone System?

SeaSpine Shoreline ACS - Anterior Cervical Standalone System is manufactured by SeaSpine Orthopedics Corporation.

What is the FDA product code for SeaSpine Shoreline ACS - Anterior Cervical Standalone System?

The FDA product code for SeaSpine Shoreline ACS - Anterior Cervical Standalone System is OVE.

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Official Source

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