Medical Device Manufacturer · US , Hillsboro , OR

Acute Innovations, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006
5
Total
5
Cleared
0
Denied

Acute Innovations, LLC has 5 FDA 510(k) cleared medical devices. Based in Hillsboro, US.

Historical record: 5 cleared submissions from 2006 to 2012. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Acute Innovations, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Acute Innovations, LLC
5 devices
1-5 of 5
Cleared Feb 17, 2012
ACUTE INNOVATIONS BIOBRIDGE RESORBABLE PLATING SYSTEM
K120163 · HRS
Orthopedic · 29d
Cleared Jan 12, 2012
ACUTE INNOVATIONS MODULAR RIBLOC SYSTEM
K113318 · HRS
Orthopedic · 63d
Cleared Sep 17, 2010
ACUTE INNOVATIONS STERNAL FIXATION SYSTEM
K101170 · KTT
Orthopedic · 144d
Cleared Sep 03, 2008
RE-ZORB PLATING SYSTEM
K081588 · HRS
Orthopedic · 90d
Cleared Jun 19, 2006
ACUTE BONE SCREW
K061206 · HWC
Orthopedic · 49d
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