Canary Tibial Extension with Canary Health Implanted Reporting Processor (CHIRP) System— 510(k) DEN200064

Name: FDA 510(k) clearance DEN200064
Creator: U.S. Food and Drug Administration
Published: 2021-08-27

Unknown

Canary Medical, Inc.

FDA 510(k) clearance DEN200064 for Canary Tibial Extension with Canary Health Implanted Reporting Processor (CHIRP) System, Unknown on 2021-08-27. Applicant: Canary Medical, Inc.. Device class: 2.

Clearance details

Applicant: Canary Medical, Inc.
Product code: Code QPP
Device class: Class 2
Regulation: 21 CFR 888.3600
Advisory panel: Orthopedic
Date received: 2020-10-19
Decision date: 2021-08-27
Decision: Unknown
Clearance type: Direct
Location: Vancouver, CA

View on FDA.gov ↗

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K234056 — canturio® se (Canturio Smart Extension)2024-04-24
K223803 — Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System2023-03-24
K220413 — Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System2022-06-22

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