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FDA 510(k)

MITRAFLEX(TM) WOUND DRESSING

K-Number: K873277 · 1987-09-17

ApplicantMatrix Medica, Inc.
Decision Date1987-09-17
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

MITRAFLEX(TM) WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Medica, Inc.. It received FDA 510(k) clearance on 1987-09-17 under 510(k) number K873277. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MITRAFLEX(TM) WOUND DRESSING?

MITRAFLEX(TM) WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1987-09-17. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K873277.

When did MITRAFLEX(TM) WOUND DRESSING receive FDA 510(k) clearance?

MITRAFLEX(TM) WOUND DRESSING received FDA 510(k) clearance on 1987-09-17, under 510(k) number K873277.

Who is the listed applicant for MITRAFLEX(TM) WOUND DRESSING?

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

What is the FDA product code for MITRAFLEX(TM) WOUND DRESSING?

The FDA product code for MITRAFLEX(TM) WOUND DRESSING is NAD.

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Related Devices (Code: NAD)

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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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