Biomet Spine (Aka Ebi, LLC)
Biomet Spine (Aka Ebi, LLC) holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2014.
Top product codes for Biomet Spine (Aka Ebi, LLC)
Recent clearances by Biomet Spine (Aka Ebi, LLC)
- K133518 — MAXAN ANTERIOR CERVICAL PLATE SYSTEM
- K140710 — BIOMET GRAFT DELIVERY SYRINGES
- K132373 — BIOMET ACCESS SYSTEM
- K133746 — POLARIS SPINAL SYSTEM
- K131615 — POLARIS SPINAL SYSTEM
- K123549 — POLARIS SPINAL SYSTEM - BALLISTA II PERCUTANEOUS SCREW PLACEMENT SYSTEM
- K123451 — POLARIS SPINAL SYSTEM - BALLISTA II RODS
- K122989 — BIOMET LATERAL SPACER SYSTEM
- K122378 — NEXTGEN ALTIUS OCT SYSTEM
- K113593 — NEXTGEN ALTIUS OCT SYSTEM
- K110650 — ZYSTON ARC INTERBODY SPACER
- K100805 — GALLERY LAMINOPLASTY FIXATION SYSTEM
- K100409 — POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTUE ANTERIOR FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.