Biomet Spine
Biomet Spine holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2016.
Top product codes for Biomet Spine
Recent clearances by Biomet Spine
- K152622 — Alta ACDF System
- K151974 — Polaris Spinal System
- K151064 — Solitaire-C Cervical Spacer System, C-Thru Anterior Spinal System, Breckenridge Small Intervertebral Body Fusion System
- K151224 — Lineum OCT Spine System
- K141791 — BIOMET FUSION SYSTEM
- K121130 — POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS
- K112014 — ZYSTON STRAIGHT SPACER SYSTEM
- K103393 — POLARIS SPINAL SYSTEM
- K093629 — SOLITAIRE AND SOLITAIRE PEEK ANTERIOR SPINAL SYSTEM
- K091067 — 5.5 POLARIS SPINAL SYSTEM
- K082793 — INTERGRO DBM
- K081952 — SYNERGY SPINAL SYSTEM (6.35 POLARIS)
- K081636 — PEEK-OPTIMA ALIF SPACER
- K081501 — SOLITAIRE ANTERIOR SPINAL SYSTEM
- K081395 — SOLITAIRE PEEK-OPTIMA ANTERIOR SPINAL SYSTEM
- K080646 — C-TEK MAXAN ANTERIOR CERVICAL PLATE SYSTEM
- K071377 — POLARIS BE RODS
- K063393 — SMALL STATURE SPACERS
- K063139 — SPINAL STABILIZING SPHERE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.