Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CoLink Plating System

K-Number: K201149 · 2020-07-15

Decision Date2020-07-15
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CoLink Plating System is a medical device manufactured by In2bones USA, LLC. It received FDA 510(k) clearance on 2020-07-15 under approval number K201149. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CoLink Plating System?

CoLink Plating System is a medical device that received FDA 510(k) clearance on 2020-07-15. It is manufactured by In2bones USA, LLC. The 510(k) number is K201149.

When was CoLink Plating System approved by the FDA?

CoLink Plating System received FDA 510(k) clearance on 2020-07-15, under approval number K201149.

What company makes CoLink Plating System?

CoLink Plating System is manufactured by In2bones USA, LLC.

What is the FDA product code for CoLink Plating System?

The FDA product code for CoLink Plating System is HRS.

Other Devices by In2bones USA, LLC

View all 25 devices →

Related Devices (Code: HRS)

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.