CTXA HIP EXTENDED REFERENCE DATA
K-Number: K030330 · 2003-06-20
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Device Summary
Frequently Asked Questions
What is the CTXA HIP EXTENDED REFERENCE DATA?
CTXA HIP EXTENDED REFERENCE DATA is a medical device that received FDA 510(k) clearance on 2003-06-20. The listed applicant is Mindways Software, Inc.. The 510(k) number is K030330.
When did CTXA HIP EXTENDED REFERENCE DATA receive FDA 510(k) clearance?
CTXA HIP EXTENDED REFERENCE DATA received FDA 510(k) clearance on 2003-06-20, under 510(k) number K030330.
Who is the listed applicant for CTXA HIP EXTENDED REFERENCE DATA?
The FDA 510(k) record lists Mindways Software, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CTXA HIP EXTENDED REFERENCE DATA?
The FDA product code for CTXA HIP EXTENDED REFERENCE DATA is KGI.
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 Mindways Software, 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.
Related Devices (Code: KGI)
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.
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