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FDA 510(k)

IBS Implant System

K-Number: K202479 · 2020-09-23

Decision Date2020-09-23
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IBS Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Innobiosurg Co., Ltd.. It received FDA 510(k) clearance on 2020-09-23 under 510(k) number K202479. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IBS Implant System?

IBS Implant System is a medical device that received FDA 510(k) clearance on 2020-09-23. The listed applicant is Innobiosurg Co., Ltd.. The 510(k) number is K202479.

When did IBS Implant System receive FDA 510(k) clearance?

IBS Implant System received FDA 510(k) clearance on 2020-09-23, under 510(k) number K202479.

Who is the listed applicant for IBS Implant System?

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

What is the FDA product code for IBS Implant System?

The FDA product code for IBS Implant System is DZE.

Other records listing Innobiosurg Co., Ltd. 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.

View all 14 devices →

Related Devices (Code: DZE)

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

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