Medical Device Manufacturer · US , Johnson City , NY

Senecka Spine - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
Denied

Senecka Spine has 2 FDA 510(k) cleared medical devices. Based in Johnson City, US.

Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Senecka Spine Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Senecka Spine
2 devices
1-2 of 2
Cleared Jan 28, 2016
Seneka II Polyscrew Pedicle Fixation System
K153525 · NKB
Orthopedic · 50d
Cleared Sep 30, 2015
Seneka I Polyscrew Pedicle Fixation System
K151849 · NKB
Orthopedic · 85d
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