SeaSpine Shoreline ACS - Anterior Cervical Standalone System
K-Number: K170569 · 2017-06-15
Device Summary
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.
Related Clinical Trials
Other Devices by SeaSpine Orthopedics Corporation
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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.