Medical Device Manufacturer · US , Minneapolis , MN

Icotec - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011
1
Total
1
Cleared
0
Denied

Icotec has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Icotec
1 devices
1-1 of 1
Cleared Jul 21, 2011
ETURN SPINAL IMPLANT MODEL ETURN XX-12
K100305 · MAX
Orthopedic · 533d
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All1 Orthopedic 1