Ellipse Technologies, Inc.
Ellipse Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2016.
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.