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FDA 510(k)

CCM Abutment System

K-Number: K173120 · 2018-03-16

Decision Date2018-03-16
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CCM Abutment 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 2018-03-16 under 510(k) number K173120. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CCM Abutment System?

CCM Abutment System is a medical device that received FDA 510(k) clearance on 2018-03-16. The listed applicant is Innobiosurg Co., Ltd.. The 510(k) number is K173120.

When did CCM Abutment System receive FDA 510(k) clearance?

CCM Abutment System received FDA 510(k) clearance on 2018-03-16, under 510(k) number K173120.

Who is the listed applicant for CCM Abutment 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 CCM Abutment System?

The FDA product code for CCM Abutment System is NHA.

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: NHA)

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.