Atlas FDA

Canary Tibial Extension with Canary Health Implanted Reporting Processor (CHIRP) System

FDA 510(k) clearance DEN200064 · decided 2021-08-27

Clearance details

K-number
DEN200064
Device name
Canary Tibial Extension with Canary Health Implanted Reporting Processor (CHIRP) System
Applicant
Canary Medical, Inc.
Decision
Unknown
Date received
2020-10-19
Decision date
2021-08-27
Days to decision
312 days
Clearance type
Direct
Product code
QPP
Device class
2
Regulation number
888.3600
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Vancouver, CA
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Canary Medical

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
canturio® se (Canturio Smart Extension) (K234056)Canary Medical USA, LLC2024-04-24
Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System (K223803)Canary Medical USA, LLC2023-03-24
Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System (K220413)Canary Medical USA, LLC2022-06-22

Recalls involving this device

No recalls on record reference this clearance.