Rebound Therapeutics

Rebound Therapeutics holds 6 FDA 510(k) medical device clearances, first cleared 2018, most recent 2021.

Top product codes for Rebound Therapeutics

GEI — General, Plastic Surgery4 devices
GWG — Neurology2 devices

Recent clearances by Rebound Therapeutics

K203745 — AURORA Evacuator +CoagCode GEI·2021-12-02
K201840 — Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box)Code GWG·2020-11-04
K201637 — Aurora Evacuator +CoagCode GEI·2020-08-12
K191861 — Aurora Surgiscope SystemCode GWG·2019-12-06
K190075 — Aurora EvacuatorCode GEI·2019-02-12
K180372 — Aurora EvacuatorCode GEI·2018-04-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.