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FDA 510(k)

DURAGEN XS DURAL REGENERATION MATRIX

K-Number: K072207 · 2007-08-23

Decision Date2007-08-23
Product CodeGXQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DURAGEN XS DURAL REGENERATION MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Integra Lifesciences Corp.. It received FDA 510(k) clearance on 2007-08-23 under 510(k) number K072207. The device is classified under product code GXQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURAGEN XS DURAL REGENERATION MATRIX?

DURAGEN XS DURAL REGENERATION MATRIX is a medical device that received FDA 510(k) clearance on 2007-08-23. The listed applicant is Integra Lifesciences Corp.. The 510(k) number is K072207.

When did DURAGEN XS DURAL REGENERATION MATRIX receive FDA 510(k) clearance?

DURAGEN XS DURAL REGENERATION MATRIX received FDA 510(k) clearance on 2007-08-23, under 510(k) number K072207.

Who is the listed applicant for DURAGEN XS DURAL REGENERATION MATRIX?

The FDA 510(k) record lists Integra Lifesciences Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DURAGEN XS DURAL REGENERATION MATRIX?

The FDA product code for DURAGEN XS DURAL REGENERATION MATRIX is GXQ.

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 Corp. 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: GXQ)

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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