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FDA 510(k)

LUCENT OR LUCENT MAGNUM

K-Number: K110632 · 2012-05-23

ApplicantSpinal Elements, Inc.
Decision Date2012-05-23
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LUCENT OR LUCENT MAGNUM is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Elements, Inc.. It received FDA 510(k) clearance on 2012-05-23 under 510(k) number K110632. 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 LUCENT OR LUCENT MAGNUM?

LUCENT OR LUCENT MAGNUM is a medical device that received FDA 510(k) clearance on 2012-05-23. The listed applicant is Spinal Elements, Inc.. The 510(k) number is K110632.

When did LUCENT OR LUCENT MAGNUM receive FDA 510(k) clearance?

LUCENT OR LUCENT MAGNUM received FDA 510(k) clearance on 2012-05-23, under 510(k) number K110632.

Who is the listed applicant for LUCENT OR LUCENT MAGNUM?

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

What is the FDA product code for LUCENT OR LUCENT MAGNUM?

The FDA product code for LUCENT OR LUCENT MAGNUM is MAX.

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Related Devices (Code: MAX)

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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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