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FDA 510(k)

ACCESS SEQUESTRATION SYSTEM

K-Number: K012406 · 2002-03-26

ApplicantInterpore Cross Intl.
Decision Date2002-03-26
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACCESS SEQUESTRATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Cross Intl.. It received FDA 510(k) clearance on 2002-03-26 under 510(k) number K012406. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESS SEQUESTRATION SYSTEM?

ACCESS SEQUESTRATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-26. The listed applicant is Interpore Cross Intl.. The 510(k) number is K012406.

When did ACCESS SEQUESTRATION SYSTEM receive FDA 510(k) clearance?

ACCESS SEQUESTRATION SYSTEM received FDA 510(k) clearance on 2002-03-26, under 510(k) number K012406.

Who is the listed applicant for ACCESS SEQUESTRATION SYSTEM?

The FDA 510(k) record lists Interpore Cross Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCESS SEQUESTRATION SYSTEM?

The FDA product code for ACCESS SEQUESTRATION SYSTEM is CAC.

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Other records listing Interpore Cross Intl. as applicant

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Related Devices (Code: CAC)

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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