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FDA 510(k)

DERMMATRIX SURGICAL MESH

K-Number: K021160 · 2002-06-12

ApplicantCarbon Medical Technologies, Inc.
Decision Date2002-06-12
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMMATRIX SURGICAL MESH is the device name listed in this FDA 510(k) record. The listed applicant is Carbon Medical Technologies, Inc.. It received FDA 510(k) clearance on 2002-06-12 under 510(k) number K021160. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMMATRIX SURGICAL MESH?

DERMMATRIX SURGICAL MESH is a medical device that received FDA 510(k) clearance on 2002-06-12. The listed applicant is Carbon Medical Technologies, Inc.. The 510(k) number is K021160.

When did DERMMATRIX SURGICAL MESH receive FDA 510(k) clearance?

DERMMATRIX SURGICAL MESH received FDA 510(k) clearance on 2002-06-12, under 510(k) number K021160.

Who is the listed applicant for DERMMATRIX SURGICAL MESH?

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

What is the FDA product code for DERMMATRIX SURGICAL MESH?

The FDA product code for DERMMATRIX SURGICAL MESH is FTM.

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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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