Summit Medventures is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Summit Medventures - FDA 510(k) Cleared Devices
Recent clearances: SMV Scientific K-Wire and Pins
2
Total
2
Cleared
0
Denied
Summit Medventures has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Summit Medventures Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Summit Medventures
2 devices