Hoogland Spine Products, GmbH

Hoogland Spine Products, GmbH holds 3 FDA 510(k) medical device clearances, first cleared 2009, most recent 2022.

Top product codes for Hoogland Spine Products, GmbH

HRX — Orthopedic2 devices
GEI — General, Plastic Surgery1 device

Recent clearances by Hoogland Spine Products, GmbH

K211173 — maxmorespine Bipolar ElectrodesCode GEI·2022-06-23
K083552 — MAXMORESPINE TOM STICKCode HRX·2009-10-09
K090132 — MAXMORESPINE SPINAL SYSTEMCode HRX·2009-06-09

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