Medical Device Manufacturer · US , Marquette , MI

Pioneer Surgical Technology, Inc. (Rti Surgical, I - FDA 510(k) Clear...

2 submissions · 2 cleared · Since 2014
2
Total
2
Cleared
0
Denied

Pioneer Surgical Technology, Inc. (Rti Surgical, I has 2 FDA 510(k) cleared medical devices. Based in Marquette, US.

Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Pioneer Surgical Technology, Inc. (Rti Surgical, I Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pioneer Surgical Technology, Inc. (Rti Surgical, I
2 devices
1-2 of 2
Cleared Oct 17, 2014
NANOSS BIOACTIVE, NANOSS BIOACTIVE LOADED, AND NANOSS BIOACTIVE LOADED KIT
K141600 · MQV
Orthopedic · 123d
Cleared Mar 19, 2014
STREAMLINE OCT OCCIPITO-CERVICO-THORACIC SYSTEM
K133374 · KWP
Orthopedic · 138d
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