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FDA 510(k)

VENUS SPINAL FIXATION SYSTEM

K-Number: K120270 · 2012-03-26

ApplicantL&K BIOMED Co., Ltd.
Decision Date2012-03-26
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VENUS SPINAL FIXATION 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 2012-03-26 under 510(k) number K120270. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENUS SPINAL FIXATION SYSTEM?

VENUS SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2012-03-26. The listed applicant is L&K BIOMED Co., Ltd.. The 510(k) number is K120270.

When did VENUS SPINAL FIXATION SYSTEM receive FDA 510(k) clearance?

VENUS SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 2012-03-26, under 510(k) number K120270.

Who is the listed applicant for VENUS SPINAL FIXATION 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 SPINAL FIXATION SYSTEM?

The FDA product code for VENUS SPINAL FIXATION SYSTEM is NKB.

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Related Devices (Code: NKB)

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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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