Facetlink Dba Linkspine is one of 18443 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Facetlink Dba Linkspine - FDA 510(k) Cleared Devices
Recent clearances: VertebraLINK Fusion Platform, CorticaLINK Spinal Fusion Platform
2
Total
2
Cleared
0
Denied
Facetlink Dba Linkspine has 2 FDA 510(k) cleared medical devices. Based in Rockaway, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Facetlink Dba Linkspine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Facetlink Dba Linkspine
2 devices