Medical Device Manufacturer · US , Parsippany , NJ

Ebi, L.P. - FDA 510(k) Cleared Devices

95 submissions · 94 cleared · Since 1997
95
Total
94
Cleared
0
Denied

Ebi, L.P. has 94 FDA 510(k) cleared orthopedic devices. Based in Parsippany, US.

Historical record: 94 cleared submissions from 1997 to 2010.

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 - Ebi, L.P.
95 devices
1-12 of 95
Cleared Jun 23, 2010
POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEM
K100438 · NKB
Orthopedic · 126d
Cleared May 17, 2010
POLARIS SPINAL SYSTEM
K100220 · NKB
Orthopedic · 111d
Cleared Apr 16, 2010
PEANUT GROWTH CONTROL PLATING SYSTEM
K093880 · HRS
Orthopedic · 119d
Cleared Feb 04, 2010
ESL SPINAL SYSTEM
K092574 · MAX
Orthopedic · 167d
Cleared Dec 01, 2009
BIOMET VISION FOOTRING SYSTEM
K093057 · KTT
Orthopedic · 62d
Cleared Oct 15, 2009
C-THRU SPINAL SYSTEM
K092336 · MQP
Orthopedic · 72d
Cleared Aug 07, 2009
IBEX SPINAL SYSTEM
K091381 · MAX
Orthopedic · 88d
Cleared Jul 30, 2009
5.5 HELICAL FLANGE SPINAL SYSTEM, POLARIS COMPONENTS
K090203 · NKB
Orthopedic · 184d
Cleared Jul 01, 2009
POLARIS SPINAL SYSTEM
K090523 · NKB
Orthopedic · 125d
Cleared Jan 14, 2009
EXPANDABLE PEEK-OPTIMA IMPLANT
K082406 · MAX
Orthopedic · 146d
Cleared Nov 13, 2008
BIOMET ANTERIOR LUMBAR PLATE
K082187 · KWQ
Orthopedic · 101d
Cleared Apr 18, 2007
PRO OSTEON 500R
K063346 · MQV
Orthopedic · 166d

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All95 Orthopedic 91 Neurology 2 Anesthesiology 2