Pioneer Surgical Technology, Inc., Dba Rti Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pioneer Surgical Technology, Inc., Dba Rti Surgical - FDA 510(k) Clea...
Recent clearances: DAC Dynamic Active Compression Plate
1
Total
1
Cleared
0
Denied
Pioneer Surgical Technology, Inc., Dba Rti Surgical has 1 FDA 510(k) cleared medical devices. Based in Marquette, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pioneer Surgical Technology, Inc., Dba Rti Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pioneer Surgical Technology, Inc., Dba Rti Surgical
1 devices