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FDA 510(k)

BIOMET CABLE SYSTEM

K-Number: K071271 · 2007-10-23

ApplicantBiomet Manufacturing, Inc.
Decision Date2007-10-23
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOMET CABLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing, Inc.. It received FDA 510(k) clearance on 2007-10-23 under 510(k) number K071271. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOMET CABLE SYSTEM?

BIOMET CABLE SYSTEM is a medical device that received FDA 510(k) clearance on 2007-10-23. The listed applicant is Biomet Manufacturing, Inc.. The 510(k) number is K071271.

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

BIOMET CABLE SYSTEM received FDA 510(k) clearance on 2007-10-23, under 510(k) number K071271.

Who is the listed applicant for BIOMET CABLE SYSTEM?

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

What is the FDA product code for BIOMET CABLE SYSTEM?

The FDA product code for BIOMET CABLE SYSTEM is JDQ.

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Other records listing Biomet Manufacturing, Inc. as applicant

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Related Devices (Code: JDQ)

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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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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