Medical Device Manufacturer · US , Washington , DC

Coalign Innovations, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2011
9
Total
9
Cleared
0
Denied

Coalign Innovations, Inc. has 9 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 9 cleared submissions from 2011 to 2013. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Coalign Innovations, Inc.
9 devices
1-9 of 9
Cleared Sep 12, 2013
ACCULIF TL AND PL CAGE
K132505 · MAX
Orthopedic · 31d
Cleared Jun 19, 2013
COALIGN INNOVATIONS ACCULIF XL IBF CAGE
K131443 · MAX
Orthopedic · 30d
Cleared Apr 03, 2013
ACCULIF XL CAGE
K130194 · MAX
Orthopedic · 65d
Cleared Jan 23, 2013
ACCULIF TL-PEEK CAGE
K123281 · MAX
Orthopedic · 93d
Cleared Jan 14, 2013
ACCULIF TL AND PL CAGE
K123752 · MAX
Orthopedic · 39d
Cleared Jul 05, 2012
ACCULIF TL CAGE
K121683 · MAX
Orthopedic · 28d
Cleared Dec 12, 2011
ACCULIF TL CAGE
K113465 · MAX
Orthopedic · 20d
Cleared Dec 01, 2011
ACCULIF TL-PEEK IBF CAGE
K112095 · MAX
Orthopedic · 132d
Cleared Apr 07, 2011
ACCULIF CAGE
K110270 · MAX
Orthopedic · 66d
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