Medical Device Manufacturer · US , Irvine , CA

Ellipse Technologies, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2011
13
Total
13
Cleared
0
Denied

Ellipse Technologies, Inc. has 13 FDA 510(k) cleared orthopedic devices. Based in Irvine, US.

Historical record: 13 cleared submissions from 2011 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 - Ellipse Technologies, Inc.
13 devices
1-12 of 13
Cleared Apr 04, 2016
PRECICE Intramedullary Limb Lengthening System
K160325 · HSB
Orthopedic · 59d
Cleared Mar 24, 2015
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
K141278 · PGN
Orthopedic · 312d
Cleared Oct 07, 2014
RESIDUAL LIMB LENGTHENING SYSTEM
K141739 · HSB
Orthopedic · 102d
Cleared Sep 18, 2014
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
K140613 · PGN
Orthopedic · 192d
Cleared Jun 30, 2014
PRECICE TRAUMA NAIL SYSTEM
K141447 · HSB
Orthopedic · 28d
Cleared May 20, 2014
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
K141023 · HSB
Orthopedic · 29d
Cleared Feb 27, 2014
ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
K140178 · PGN
Orthopedic · 34d
Cleared Jan 23, 2014
ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
K131490 · HSB
Orthopedic · 245d
Cleared Dec 09, 2013
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
K133289 · HSB
Orthopedic · 45d
Cleared Oct 11, 2013
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
K131677 · HSB
Orthopedic · 123d
Cleared Oct 19, 2012
ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
K113219 · HSB
Orthopedic · 353d
Cleared Mar 28, 2012
ELLIPSE PRECICE TRAUMA NAIL SYSTEM
K113695 · HSB
Orthopedic · 103d
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