ENDIUS TITLE SPINAL FIXATION SYSTEM
K-Number: K021881 · 2002-07-29
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Device Summary
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.
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
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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