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FDA 510(k)

PERMARIDGE HYDROXYLAPATITE MATRIX

K-Number: K960349 · 1996-03-13

ApplicantCeramed Corp.
Decision Date1996-03-13
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERMARIDGE HYDROXYLAPATITE MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Ceramed Corp.. It received FDA 510(k) clearance on 1996-03-13 under 510(k) number K960349. 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 PERMARIDGE HYDROXYLAPATITE MATRIX?

PERMARIDGE HYDROXYLAPATITE MATRIX is a medical device that received FDA 510(k) clearance on 1996-03-13. The listed applicant is Ceramed Corp.. The 510(k) number is K960349.

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

PERMARIDGE HYDROXYLAPATITE MATRIX received FDA 510(k) clearance on 1996-03-13, under 510(k) number K960349.

Who is the listed applicant for PERMARIDGE HYDROXYLAPATITE MATRIX?

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

What is the FDA product code for PERMARIDGE HYDROXYLAPATITE MATRIX?

The FDA product code for PERMARIDGE HYDROXYLAPATITE MATRIX is FWP.

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Other records listing Ceramed 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.

K962838PERMARIDGE SYRINGEK962786OSTEOGRAF STAINLESS STEEL SYRINGK960348OSTEOGRAF/N-300 HYDROXYLAPATITEK960368OSTEOGRAFT/N-700 HYDROXYLAPTITEK960353OSTEOGRAF/LD-300 HYDROXYLAPATITEK960361PERMAMESH-D HYDROXYLAPATITE MATRIX

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Related Devices (Code: FWP)

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K254233MEDPOR Customized Implant KitStryker Leibinger GmbH & Co KGK232593FITme Customized Silicone ImplantKeosan Trading Co.K200610Customized Contour ImplantImplantech Associates, Inc.K191130Customized Contour ImplantImplantech Associates, Inc.K191916Stryker CMF MEDPOR Priority Customized Implant KitStryker Leibinger GmbH & Co KGK153508Stryker CMF MEDPOR Customized ImplantStryker

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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