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FDA 510(k)

CC-Clip® Implant System

K-Number: K232780 · 2023-12-18

ApplicantCc-Instruments, Inc.
Decision Date2023-12-18
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CC-Clip® Implant System is a medical device manufactured by Cc-Instruments, Inc.. It received FDA 510(k) clearance on 2023-12-18 under approval 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. It is manufactured by Cc-Instruments, Inc.. The 510(k) number is K232780.

When was CC-Clip® Implant System approved by the FDA?

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

What company makes CC-Clip® Implant System?

CC-Clip® Implant System is manufactured by Cc-Instruments, Inc..

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

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

Related Clinical Trials

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Related PubMed Literature

PMID: 41966145 From Registry to Reality: Opportunities to Enhance Post-market Surveillance of High-Risk Medical Devices Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review". International journal of health policy and management (2025)

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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.

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