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)

Navident

K-Number: K233563 · 2024-07-25

ApplicantClaronav, Inc.
Decision Date2024-07-25
Product CodePLV
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Navident is a medical device manufactured by Claronav, Inc.. It received FDA 510(k) clearance on 2024-07-25 under approval number K233563. The device is classified under product code PLV. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Navident?

Navident is a medical device that received FDA 510(k) clearance on 2024-07-25. It is manufactured by Claronav, Inc.. The 510(k) number is K233563.

When was Navident approved by the FDA?

Navident received FDA 510(k) clearance on 2024-07-25, under approval number K233563.

What company makes Navident?

Navident is manufactured by Claronav, Inc..

What is the FDA product code for Navident?

The FDA product code for Navident is PLV.

Other Devices by Claronav, Inc.

K161406Navident K163439NaviENT K210947Navident

Related Devices (Code: PLV)

K161399Neocis Guidance SystemNeocis, Inc. K161406NavidentClaronav, Inc. K182776Neocis Guidance SystemNeocis, Inc. K173402Neocis Guidance System (NGS) with Chairside SplintNeocis, Inc. K191363Neocis Planning Software Application (NPSA) for 3rd Party PCsNeocis, Inc. K191605Neocis Guidance System (NGS)Neocis, Inc.

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.

↑