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FDA 510(k)

LUCENT MAGNUM

K-Number: K083475 · 2009-02-13

ApplicantSpinal Elements, Inc.
Decision Date2009-02-13
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 2009-02-13 under 510(k) number K083475. 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 2009-02-13. The listed applicant is Spinal Elements, Inc.. The 510(k) number is K083475.

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

LUCENT MAGNUM received FDA 510(k) clearance on 2009-02-13, under 510(k) number K083475.

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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