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FDA 510(k)

INNERVUE DIAGNOSTIC SCOPE SYSTEM

K-Number: K072879 · 2008-01-14

ApplicantBiomet Orthopedics, Inc.
Decision Date2008-01-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INNERVUE DIAGNOSTIC SCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2008-01-14 under 510(k) number K072879. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNERVUE DIAGNOSTIC SCOPE SYSTEM?

INNERVUE DIAGNOSTIC SCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-01-14. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K072879.

When did INNERVUE DIAGNOSTIC SCOPE SYSTEM receive FDA 510(k) clearance?

INNERVUE DIAGNOSTIC SCOPE SYSTEM received FDA 510(k) clearance on 2008-01-14, under 510(k) number K072879.

Who is the listed applicant for INNERVUE DIAGNOSTIC SCOPE SYSTEM?

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

What is the FDA product code for INNERVUE DIAGNOSTIC SCOPE SYSTEM?

The FDA product code for INNERVUE DIAGNOSTIC SCOPE SYSTEM is HRX.

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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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