Biomet Spine (Aka Ebi, LLC) - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Biomet Spine (Aka Ebi, LLC) has 13 FDA 510(k) cleared orthopedic devices. Based in Parsippany, US.
Historical record: 13 cleared submissions from 2010 to 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Nov 05, 2014
MAXAN ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
355d
Cleared
Sep 04, 2014
BIOMET GRAFT DELIVERY SYRINGES
General Hospital
167d
Cleared
Mar 27, 2014
BIOMET ACCESS SYSTEM
Neurology
240d
Cleared
Mar 12, 2014
POLARIS SPINAL SYSTEM
Orthopedic
93d
Cleared
Sep 04, 2013
POLARIS SPINAL SYSTEM
Orthopedic
93d
Cleared
Feb 25, 2013
POLARIS SPINAL SYSTEM - BALLISTA II PERCUTANEOUS SCREW PLACEMENT SYSTEM
Orthopedic
98d
Cleared
Dec 03, 2012
POLARIS SPINAL SYSTEM - BALLISTA II RODS
Orthopedic
24d
Cleared
Oct 24, 2012
BIOMET LATERAL SPACER SYSTEM
Orthopedic
28d
Cleared
Sep 20, 2012
NEXTGEN ALTIUS OCT SYSTEM
Orthopedic
45d
Cleared
Apr 17, 2012
NEXTGEN ALTIUS OCT SYSTEM
Orthopedic
134d
Cleared
Jun 30, 2011
ZYSTON ARC INTERBODY SPACER
Orthopedic
118d
Cleared
Jul 20, 2010
GALLERY LAMINOPLASTY FIXATION SYSTEM
Orthopedic
120d
Cleared
Jun 23, 2010
POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTUE ANTERIOR FIXATION SYSTEM
Orthopedic
127d