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FDA 510(k)

CORIOGRAPH Pre-Op Planning and Modeling Services

K-Number: K242272 · 2024-11-15

Decision Date2024-11-15
Product Code
DecisionSubstantially Equivalent

Device Summary

CORIOGRAPH Pre-Op Planning and Modeling Services is the device name listed in this FDA 510(k) record. The listed applicant is Blue Belt Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-15 under 510(k) 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. 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.

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Official Source

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