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)

Reliance Cervical IBF System

K-Number: K202266 · 2022-03-29

Decision Date2022-03-29
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Reliance Cervical IBF System is a medical device manufactured by Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2022-03-29 under approval number K202266. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reliance Cervical IBF System?

Reliance Cervical IBF System is a medical device that received FDA 510(k) clearance on 2022-03-29. It is manufactured by Reliance Medical Systems, LLC. The 510(k) number is K202266.

When was Reliance Cervical IBF System approved by the FDA?

Reliance Cervical IBF System received FDA 510(k) clearance on 2022-03-29, under approval number K202266.

What company makes Reliance Cervical IBF System?

Reliance Cervical IBF System is manufactured by Reliance Medical Systems, LLC.

What is the FDA product code for Reliance Cervical IBF System?

The FDA product code for Reliance Cervical IBF System is ODP.

Related Clinical Trials

Other Devices by Reliance Medical Systems, LLC

View all 8 devices →

Related Devices (Code: ODP)

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.