Ellipse Technologies, Inc.
FDA 510(k) medical device clearances.
Top product codes for Ellipse Technologies, Inc.
Recent clearances by Ellipse Technologies, Inc.
- K160325 — PRECICE Intramedullary Limb Lengthening System
- K141278 — MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
- K141739 — RESIDUAL LIMB LENGTHENING SYSTEM
- K140613 — MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
- K141447 — PRECICE TRAUMA NAIL SYSTEM
- K141023 — PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
- K140178 — ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
- K131490 — ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
- K133289 — PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
- K131677 — PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
- K113219 — ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
- K113695 — ELLIPSE PRECICE TRAUMA NAIL SYSTEM
- K101997 — ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.