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FDA 510(k)

LUCENT MAGNUM+

K-Number: K081711 · 2008-09-11

ApplicantSpinal Elements, Inc.
Decision Date2008-09-11
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

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 2008-09-11 under 510(k) number K081711. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUCENT MAGNUM+?

LUCENT MAGNUM+ is a medical device that received FDA 510(k) clearance on 2008-09-11. The listed applicant is Spinal Elements, Inc.. The 510(k) number is K081711.

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

LUCENT MAGNUM+ received FDA 510(k) clearance on 2008-09-11, under 510(k) number K081711.

Who is the listed applicant for 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 MAGNUM+?

The FDA product code for LUCENT MAGNUM+ is OVD.

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Related Devices (Code: OVD)

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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