Navident— 510(k) K161406

Substantially Equivalent

Claronav, Inc.

FDA 510(k) clearance K161406 for Navident, Substantially Equivalent on 2016-09-08. Applicant: Claronav, Inc.. Device class: 2.

Clearance details

Applicant: Claronav, Inc.
Product code: Code PLV
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2016-05-20
Decision date: 2016-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toronto, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code PLV

K252376 — Yomi S Robotic System2025-10-28
K251835 — Yomi Robotic System2025-10-10
K233563 — Navident2024-07-25
K231018 — Yomi Robotic System2023-08-14
K210947 — Navident2022-06-27

More clearances from Claronav, Inc.

K163439 — NaviENT2017-09-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.