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FDA 510(k)

THE PERMARIDGE MATRIX CHIN

K-Number: K931500 · 1994-11-17

ApplicantApplied Biomaterial Technologies
Decision Date1994-11-17
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE PERMARIDGE MATRIX CHIN is the device name listed in this FDA 510(k) record. The listed applicant is Applied Biomaterial Technologies. It received FDA 510(k) clearance on 1994-11-17 under 510(k) number K931500. The device is classified under product code FWP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PERMARIDGE MATRIX CHIN?

THE PERMARIDGE MATRIX CHIN is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is Applied Biomaterial Technologies. The 510(k) number is K931500.

When did THE PERMARIDGE MATRIX CHIN receive FDA 510(k) clearance?

THE PERMARIDGE MATRIX CHIN received FDA 510(k) clearance on 1994-11-17, under 510(k) number K931500.

Who is the listed applicant for THE PERMARIDGE MATRIX CHIN?

The FDA 510(k) record lists Applied Biomaterial Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE PERMARIDGE MATRIX CHIN?

The FDA product code for THE PERMARIDGE MATRIX CHIN is FWP.

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Other records listing Applied Biomaterial Technologies 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: FWP)

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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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