Signus Medizintechnik GmbH
FDA 510(k) medical device clearances.
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.