免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Zimmer M/L Taper Hip Prosthesis

K号: K161830 · 2016-10-26

申请人Zimmer, Inc.
决定日期2016-10-26
产品代码LZO
咨询委员会OR
决定Substantially Equivalent

器械摘要

Zimmer M/L Taper Hip Prosthesis is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2016-10-26 under 510(k) number K161830. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Zimmer M/L Taper Hip Prosthesis?

Zimmer M/L Taper Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2016-10-26. The listed applicant is Zimmer, Inc.. The 510(k) number is K161830.

When did Zimmer M/L Taper Hip Prosthesis receive FDA 510(k) clearance?

Zimmer M/L Taper Hip Prosthesis received FDA 510(k) clearance on 2016-10-26, under 510(k) number K161830.

Who is the listed applicant for Zimmer M/L Taper Hip Prosthesis?

The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zimmer M/L Taper Hip Prosthesis?

The FDA product code for Zimmer M/L Taper Hip Prosthesis is LZO.

相关临床试验

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

列明Zimmer, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

查看所有 61 个设备 →

相关器械(代码:LZO)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。

↑