CORIOGRAPH Pre-Op Planning and Modeling Services
K-Number: K242272 · 2024-11-15
ApplicantBlue Belt Technologies, Inc.
Decision Date2024-11-15
Product Code
DecisionSubstantially Equivalent
Device Summary
CORIOGRAPH Pre-Op Planning and Modeling Services is a medical device manufactured by Blue Belt Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-15 under approval number K242272. FDA Decision: Substantially Equivalent.
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. It is manufactured by Blue Belt Technologies, Inc.. The 510(k) number is K242272.
When was CORIOGRAPH Pre-Op Planning and Modeling Services approved by the FDA?
CORIOGRAPH Pre-Op Planning and Modeling Services received FDA 510(k) clearance on 2024-11-15, under approval number K242272.
What company makes CORIOGRAPH Pre-Op Planning and Modeling Services?
CORIOGRAPH Pre-Op Planning and Modeling Services is manufactured by Blue Belt Technologies, Inc..
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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.