Spr Therapeutics, LLC is one of 21901 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spr Therapeutics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Sprint System, Single Procedure Kit, Sprint System with Pad II, Single Procedure Kit, Sprint System, Multi-Procedure Kit, Sprint System, Sterile Components Kit, Sprint System, Stimulator Kit, Smartpatch PNS MicroLead and Accessories, Smartpatch PNS Stimulator, Pads, and Accessories, Smartpatch PNS MicroLead and Introducer, Smartpatch PNS Pads, 4 Packs
2
Total
2
Cleared
0
Denied
Spr Therapeutics, LLC has 2 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Spr Therapeutics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sfa Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Spr Therapeutics, LLC
2 devices