Spark Neuro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spark Neuro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPARK Scan
1
Total
1
Cleared
0
Denied
Spark Neuro, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Spark Neuro, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Spark Neuro, Inc.
1 devices