KLOCKNER SURGICAL BOX
K-Number: K173642 · 2018-10-02
Device Summary
Frequently Asked Questions
What is the KLOCKNER SURGICAL BOX?
KLOCKNER SURGICAL BOX is a medical device that received FDA 510(k) clearance on 2018-10-02. The listed applicant is SOADCO, S.L.. The 510(k) number is K173642.
When did KLOCKNER SURGICAL BOX receive FDA 510(k) clearance?
KLOCKNER SURGICAL BOX received FDA 510(k) clearance on 2018-10-02, under 510(k) number K173642.
Who is the listed applicant for KLOCKNER SURGICAL BOX?
The FDA 510(k) record lists SOADCO, S.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KLOCKNER SURGICAL BOX?
The FDA product code for KLOCKNER SURGICAL BOX is KCT.
Other records listing SOADCO, S.L. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.