Creaspine is one of 24549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Creaspine - FDA 510(k) Cleared Devices
Recent clearances: CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM LINE EXTENSION, CREASPINE SUPSTANCE SMALL VERTEBRAL BODY REPLACEMENT SYSTEM
2
Total
2
Cleared
0
Denied
Creaspine has 2 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 2 cleared submissions from 2008 to 2008. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Creaspine Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Creaspine
2 devices