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FDA 510(k)

LUCENT

K-Number: K071724 · 2007-11-09

ApplicantSpinal Elements, Inc.
Decision Date2007-11-09
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LUCENT 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 2007-11-09 under 510(k) number K071724. 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?

LUCENT is a medical device that received FDA 510(k) clearance on 2007-11-09. The listed applicant is Spinal Elements, Inc.. The 510(k) number is K071724.

When did LUCENT receive FDA 510(k) clearance?

LUCENT received FDA 510(k) clearance on 2007-11-09, under 510(k) number K071724.

Who is the listed applicant for LUCENT?

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?

The FDA product code for LUCENT is MAX.

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Other records listing Spinal Elements, Inc. as applicant

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Related Devices (Code: MAX)

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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