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FDA 510(k)

ENDIUS TITLE SPINAL FIXATION SYSTEM

K-Number: K021881 · 2002-07-29

ApplicantEndius, Inc.
Decision Date2002-07-29
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ENDIUS TITLE SPINAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Endius, Inc.. It received FDA 510(k) clearance on 2002-07-29 under 510(k) number K021881. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDIUS TITLE SPINAL FIXATION SYSTEM?

ENDIUS TITLE SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-29. The listed applicant is Endius, Inc.. The 510(k) number is K021881.

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

ENDIUS TITLE SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 2002-07-29, under 510(k) number K021881.

Who is the listed applicant for ENDIUS TITLE SPINAL FIXATION SYSTEM?

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

What is the FDA product code for ENDIUS TITLE SPINAL FIXATION SYSTEM?

The FDA product code for ENDIUS TITLE SPINAL FIXATION SYSTEM is MNH. This falls under the ENT category.

Related Clinical Trials

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.

Other records listing Endius, Inc. as applicant

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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Related Devices (Code: MNH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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