FDA 510(k)

CC-Clip® Implant System

K-Number: K232780 · 2023-12-18

Decision Date2023-12-18

Product CodeHTN

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CC-Clip® Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Cc-Instruments, Inc.. It received FDA 510(k) clearance on 2023-12-18 under 510(k) number K232780. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CC-Clip® Implant System?

CC-Clip® Implant System is a medical device that received FDA 510(k) clearance on 2023-12-18. The listed applicant is Cc-Instruments, Inc.. The 510(k) number is K232780.

When did CC-Clip® Implant System receive FDA 510(k) clearance?

CC-Clip® Implant System received FDA 510(k) clearance on 2023-12-18, under 510(k) number K232780.

Who is the listed applicant for CC-Clip® Implant System?

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

What is the FDA product code for CC-Clip® Implant System?

The FDA product code for CC-Clip® Implant System is HTN.

Related Devices (Code: HTN)

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.

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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.