Icotec AG
FDA 510(k) medical device clearances.
Top product codes for Icotec AG
Recent clearances by Icotec AG
- K252327 — CMORE® CT System; CMORE® CT System Navigated Instruments
- K242900 — VADER® Pedicle System and VADER®one Pedicle System
- K233215 — icotec Anterior Cervical Plate System
- K232792 — icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn TLIF Lumbar Cage)
- K232790 — KONG®-TL VBR System and KONG® C VBR System
- K232628 — VADER® Pedicle System
- K230861 — VADER® Pedicle System Navigated Instruments
- K222789 — VADER® Pedicle System, G21 Cement
- K201587 — icotec Anterior Cervical Plate System
- K200596 — G21 Cement, VADER® Pedicle System
- K200235 — KONG-TL VBR System, KONG-C VBR System
- K193423 — VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0
- K192897 — icotec Cervical Cage
- K190545 — VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0
- K172480 — icotec Interbody Cage System
- K151977 — icotec Pedicle System
Data sourced from openFDA. This site is unofficial and independent of the FDA.