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FDA 510(k)

VITREA ENDOVASCULAR STENT PLANNING SOFTWARE

K-Number: K091498 · 2009-06-05

Decision Date2009-06-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VITREA ENDOVASCULAR STENT PLANNING SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Images, Inc.. It received FDA 510(k) clearance on 2009-06-05 under 510(k) number K091498. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITREA ENDOVASCULAR STENT PLANNING SOFTWARE?

VITREA ENDOVASCULAR STENT PLANNING SOFTWARE is a medical device that received FDA 510(k) clearance on 2009-06-05. The listed applicant is Vital Images, Inc.. The 510(k) number is K091498.

When did VITREA ENDOVASCULAR STENT PLANNING SOFTWARE receive FDA 510(k) clearance?

VITREA ENDOVASCULAR STENT PLANNING SOFTWARE received FDA 510(k) clearance on 2009-06-05, under 510(k) number K091498.

Who is the listed applicant for VITREA ENDOVASCULAR STENT PLANNING SOFTWARE?

The FDA 510(k) record lists Vital Images, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITREA ENDOVASCULAR STENT PLANNING SOFTWARE?

The FDA product code for VITREA ENDOVASCULAR STENT PLANNING SOFTWARE is LLZ.

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 Vital Images, 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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Related Devices (Code: LLZ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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