INTEGRA BONE FIXATION SYSTEM
K-Number: K040860 · 2004-06-17
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Device Summary
Frequently Asked Questions
What is the INTEGRA BONE FIXATION SYSTEM?
INTEGRA BONE FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2004-06-17. The listed applicant is Integra LifeSciences Corporation. The 510(k) number is K040860.
When did INTEGRA BONE FIXATION SYSTEM receive FDA 510(k) clearance?
INTEGRA BONE FIXATION SYSTEM received FDA 510(k) clearance on 2004-06-17, under 510(k) number K040860.
Who is the listed applicant for INTEGRA BONE FIXATION SYSTEM?
The FDA 510(k) record lists Integra LifeSciences Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTEGRA BONE FIXATION SYSTEM?
The FDA product code for INTEGRA BONE FIXATION SYSTEM is HRS.
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 Integra LifeSciences Corporation 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: HRS)
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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