FDA 510(k)

SEC VBR

K-Number: K091743 · 2009-11-02

Decision Date2009-11-02

Product CodeMQP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SEC VBR is the device name listed in this FDA 510(k) record. The listed applicant is Innvotec Surgical, Inc.. It received FDA 510(k) clearance on 2009-11-02 under 510(k) number K091743. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEC VBR?

SEC VBR is a medical device that received FDA 510(k) clearance on 2009-11-02. The listed applicant is Innvotec Surgical, Inc.. The 510(k) number is K091743.

When did SEC VBR receive FDA 510(k) clearance?

SEC VBR received FDA 510(k) clearance on 2009-11-02, under 510(k) number K091743.

Who is the listed applicant for SEC VBR?

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

What is the FDA product code for SEC VBR?

The FDA product code for SEC VBR is MQP.

Other records listing Innvotec Surgical, 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.

K093669SEC IBF CAGE

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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.