CORIOGRAPH Pre-Op Planning and Modeling Services
K-Number: K242272 · 2024-11-15
Device Summary
Frequently Asked Questions
What is the CORIOGRAPH Pre-Op Planning and Modeling Services?
CORIOGRAPH Pre-Op Planning and Modeling Services is a medical device that received FDA 510(k) clearance on 2024-11-15. The listed applicant is Blue Belt Technologies, Inc.. The 510(k) number is K242272.
When did CORIOGRAPH Pre-Op Planning and Modeling Services receive FDA 510(k) clearance?
CORIOGRAPH Pre-Op Planning and Modeling Services received FDA 510(k) clearance on 2024-11-15, under 510(k) number K242272.
Who is the listed applicant for CORIOGRAPH Pre-Op Planning and Modeling Services?
The FDA 510(k) record lists Blue Belt Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Blue Belt Technologies, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.