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FDA 510(k)

COSMATRIX

K-Number: K060829 · 2006-05-17

ApplicantTei Biosciences, Inc.
Decision Date2006-05-17
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COSMATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Tei Biosciences, Inc.. It received FDA 510(k) clearance on 2006-05-17 under 510(k) number K060829. 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 COSMATRIX?

COSMATRIX is a medical device that received FDA 510(k) clearance on 2006-05-17. The listed applicant is Tei Biosciences, Inc.. The 510(k) number is K060829.

When did COSMATRIX receive FDA 510(k) clearance?

COSMATRIX received FDA 510(k) clearance on 2006-05-17, under 510(k) number K060829.

Who is the listed applicant for COSMATRIX?

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

What is the FDA product code for COSMATRIX?

The FDA product code for COSMATRIX is FTM.

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Other records listing Tei Biosciences, Inc. as applicant

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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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