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# FDA Clears SeaSpine’s Anterior Cervical System
- URL: https://www.fdaweb.com/fda-clears-seaspines-anterior-cervical-system/
- Published: 2016-10-27T12:00:00.000Z
- Updated: 2026-09-14T21:43:12.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5137194

FDA has cleared a SeaSpine Holdings 510(k) for its Shoreline ACS Anterior Cervical Standalone System, which features TruProfile technology. The device offers a low profile plate that is designed to minimize cephalad-caudal encroachment onto the vertebral bodies and maximize the distance from adjacent disc spaces, according to the company. It is designed to maximize intraoperative flexibility by offering a complement of zero and low-profile plating options, including two-, three- and four-hole variations, as well as 10 degree lordotic implants, it says.