Signus Medizintechnik GmbH
Signus Medizintechnik GmbH holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2025.
Top product codes for Signus Medizintechnik GmbH
Recent clearances by Signus Medizintechnik GmbH
- K243188 — CYLOX® ST
- K241438 — Signus Tetris St; Signus Tetris R St
- K220658 — COSY Cervicothoracic Occipital Rod-Screw System
- K212755 — SIGNUS SACRONAIL® Transsacral Stabilization System
- K151704 — Diplomat® Spinal System
- K141405 — MOBIS II ST SPINAL IMPLANT
- K123758 — TASMIN R
- K131372 — MOBIS II
- K122317 — TETRIS II
- K111792 — MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI
- K090387 — KAINOS+
- K082848 — NUBIC AND RABEA DEVICES
- K081332 — ATHLET VERTEBRAL BODY REPLACEMENT SYSTEM
- K080815 — TOSCA II ANTERIOR CERVICAL PLATE SYSTEM
- K080349 — KIMBA MINI
- K061082 — MOBIS SPINAL IMPLANT
- K061577 — OVALTWIST PEDICLE SCREW SYSTEM
- K052533 — KIMBA SPINAL IMPLANT
- K051659 — SEMIAL SPINAL IMPLANT
- K043316 — RABEA SPINAL IMPLANT
- K043082 — THE TOSCA ANTERIOR CERVICAL PLATE SYSTEM
- K041888 — CURVED PEEK TETRIS SPINAL IMPLANT
- K990345 — RABEA DEVICE, MODEL PXXXXXX
Data sourced from openFDA. This site is unofficial and independent of the FDA.