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FDA 510(k)

RIDGEMATRIX 20/40 MESH, PERIOMATRIX

K-Number: K842163 · 1984-08-09

Decision Date1984-08-09
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RIDGEMATRIX 20/40 MESH, PERIOMATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Orthomatrix, Inc.. It received FDA 510(k) clearance on 1984-08-09 under 510(k) number K842163. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIDGEMATRIX 20/40 MESH, PERIOMATRIX?

RIDGEMATRIX 20/40 MESH, PERIOMATRIX is a medical device that received FDA 510(k) clearance on 1984-08-09. The listed applicant is Orthomatrix, Inc.. The 510(k) number is K842163.

When did RIDGEMATRIX 20/40 MESH, PERIOMATRIX receive FDA 510(k) clearance?

RIDGEMATRIX 20/40 MESH, PERIOMATRIX received FDA 510(k) clearance on 1984-08-09, under 510(k) number K842163.

Who is the listed applicant for RIDGEMATRIX 20/40 MESH, PERIOMATRIX?

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

What is the FDA product code for RIDGEMATRIX 20/40 MESH, PERIOMATRIX?

The FDA product code for RIDGEMATRIX 20/40 MESH, PERIOMATRIX is LYC.

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 Orthomatrix, Inc. 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.

View all 8 devices →

Related Devices (Code: LYC)

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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