FDA 510(k)

Unison-C 頸椎前方固定系統

K 號：K170830 · 2017-06-28

申請人Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc.

決定日期2017-06-28

產品代碼OVE

諮詢委員會或

決定相當於

器材摘要

Unison-C Anterior Cervical Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc.. It received FDA 510(k) clearance on 2017-06-28 under 510(k) number K170830. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Unison-C Anterior Cervical Fixation System?

Unison-C Anterior Cervical Fixation System is a medical device that received FDA 510(k) clearance on 2017-06-28. The listed applicant is Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc.. The 510(k) number is K170830.

When did Unison-C Anterior Cervical Fixation System receive FDA 510(k) clearance?

Unison-C Anterior Cervical Fixation System received FDA 510(k) clearance on 2017-06-28, under 510(k) number K170830.

Who is the listed applicant for Unison-C Anterior Cervical Fixation System?

The FDA 510(k) record lists Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Unison-C Anterior Cervical Fixation System?

The FDA product code for Unison-C Anterior Cervical Fixation System is OVE.