Biomet Spine (Aka Ebi, LLC)
FDA 510(k) medical device clearances.
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.