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FDA 510(k)

BIOMET VISION FOOTRING SYSTEM

K-Number: K071395 · 2007-07-09

ApplicantBiomet Manufacturing Corp
Decision Date2007-07-09
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOMET VISION FOOTRING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2007-07-09 under 510(k) number K071395. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOMET VISION FOOTRING SYSTEM?

BIOMET VISION FOOTRING SYSTEM is a medical device that received FDA 510(k) clearance on 2007-07-09. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K071395.

When did BIOMET VISION FOOTRING SYSTEM receive FDA 510(k) clearance?

BIOMET VISION FOOTRING SYSTEM received FDA 510(k) clearance on 2007-07-09, under 510(k) number K071395.

Who is the listed applicant for BIOMET VISION FOOTRING SYSTEM?

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

What is the FDA product code for BIOMET VISION FOOTRING SYSTEM?

The FDA product code for BIOMET VISION FOOTRING SYSTEM is KTT.

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Related Devices (Code: KTT)

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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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