FDA 510(k)

VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM

K-Number: K121096 · 2012-07-06

Decision Date2012-07-06

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is L&K BIOMED Co., Ltd.. It received FDA 510(k) clearance on 2012-07-06 under 510(k) number K121096. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM?

VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM is a medical device that received FDA 510(k) clearance on 2012-07-06. The listed applicant is L&K BIOMED Co., Ltd.. The 510(k) number is K121096.

When did VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM receive FDA 510(k) clearance?

VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM received FDA 510(k) clearance on 2012-07-06, under 510(k) number K121096.

Who is the listed applicant for VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM?

The FDA 510(k) record lists L&K BIOMED Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM?

The FDA product code for VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM is MAX.

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Related Devices (Code: MAX)

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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.