FDA 510(k)

KLOCKNER SURGICAL BOX

K-Number: K173642 · 2018-10-02

Decision Date2018-10-02

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

KLOCKNER SURGICAL BOX is a medical device manufactured by SOADCO, S.L.. It received FDA 510(k) clearance on 2018-10-02 under approval number K173642. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by SOADCO, S.L.. The 510(k) number is K173642.

When was KLOCKNER SURGICAL BOX approved by the FDA?

KLOCKNER SURGICAL BOX received FDA 510(k) clearance on 2018-10-02, under approval number K173642.

What company makes KLOCKNER SURGICAL BOX?

KLOCKNER SURGICAL BOX is manufactured by SOADCO, S.L..

What is the FDA product code for KLOCKNER SURGICAL BOX?

The FDA product code for KLOCKNER SURGICAL BOX is KCT.

Other Devices by SOADCO, S.L.

K153098KLOCKNER VEGA DENTAL IMPLANT SYSTEM K151194KLOCKNER DENTAL IMPLANT ABUTMENTS (II) K170022Klockner Vega TiBase for CEREC K230103Klockner Abutments K243128Klockner Kits

Related Devices (Code: KCT)

K160574K3PRO SURGICAL TRAYArgon Med. Productions Vertriebs Gesellschaft Mbh CO KG K162600Jewel Precision Reusable Rigid Sterilization Container SystemJewel Precision Sheet Metal & Machine, Inc. K160912Sterilization TraySTERIS Corporation K161347Signia sterilization trayCovidien K152745ReNew Sterilization Trays(Catalog #3708 and #3709)Microline Surgical, Inc. K152111Symmetry Surgical Quad-Lock Container SystemSymmetry Surgical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.