Medical Device Manufacturer · US , Washington , DC

Paradigm Spine, LLC - FDA 510(k) Cleared Devices

11 submissions · 4 cleared · Since 2008
11
Total
4
Cleared
0
Denied

Paradigm Spine, LLC has 4 FDA 510(k) cleared orthopedic devices. Based in Washington, US.

Historical record: 4 cleared submissions from 2008 to 2016.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Paradigm Spine, LLC
11 devices
1-11 of 11
Cleared Sep 08, 2016
coflex-IF
K153302 · PEK
Orthopedic · 300d
Cleared May 09, 2012
DSS STABILIZATION SYSTEM-RIGID
K120491 · MNH
Orthopedic · 82d
Cleared Feb 13, 2012
COFLEX-F
K112595 · KWP
Orthopedic · 159d
Cleared Jan 10, 2012
DSS STABILIZATION SYSTEM
K113625 · NKB
Orthopedic · 33d
Cleared Oct 06, 2010
PARADIGM INTERSPINOUS FUSION PLATE
K093438 · KWP
Orthopedic · 336d
Cleared Jul 02, 2010
DSS STABILIZATION SYSTEM
K101083 · NQP
Orthopedic · 74d
Cleared Aug 03, 2009
MODIFICATION TO: DSS STABILIZATION SYSTEM
K091944 · NQP
Orthopedic · 34d
Cleared Jun 19, 2009
DSS STABILIZATION SYSTEM
K090099 · NKB
Orthopedic · 155d
Cleared Mar 20, 2009
MODIFICATION TO: DSS STABILIZATION SYSTEM
K090408 · NKB
Orthopedic · 30d
Cleared Nov 28, 2008
DDS STABILIZATION SYSTEM
K080241 · NQP
Orthopedic · 302d
Cleared Jan 24, 2008
DSS
K072969 · NQP
Orthopedic · 94d
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