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FDA 510(k)

BONEVUE

K-Number: K083691 · 2009-02-25

ApplicantMicromri, Inc.
Decision Date2009-02-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BONEVUE is the device name listed in this FDA 510(k) record. The listed applicant is Micromri, Inc.. It received FDA 510(k) clearance on 2009-02-25 under 510(k) number K083691. 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 BONEVUE?

BONEVUE is a medical device that received FDA 510(k) clearance on 2009-02-25. The listed applicant is Micromri, Inc.. The 510(k) number is K083691.

When did BONEVUE receive FDA 510(k) clearance?

BONEVUE received FDA 510(k) clearance on 2009-02-25, under 510(k) number K083691.

Who is the listed applicant for BONEVUE?

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

What is the FDA product code for BONEVUE?

The FDA product code for BONEVUE is LLZ.

Related Clinical Trials

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Other records listing Micromri, 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.

K073131MICROMRI WRIST COIL

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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.

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