Bk Meditech, Co., Ltd.
Bk Meditech, Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2020.
Top product codes for Bk Meditech, Co., Ltd.
Recent clearances by Bk Meditech, Co., Ltd.
- K200981 — Mega Plus MIS Spine System
- K183080 — Mega Plus Spine System
- K173180 — Mega Plus Spine System
- K140577 — INNESIS PEEK TL CAGE
- K132483 — INNESIS PEEK CERVICAL CAGE
- K120464 — INNESIS PEEK CAGE
- K110426 — DYNA-EXTOR II
- K090424 — DVX SPINE SYSTEM
- K080876 — DVX SPINE SYSTEM
- K072436 — MEGA SPINE SYSTEM
- K061599 — PIN SCREW
Data sourced from openFDA. This site is unofficial and independent of the FDA.