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FDA 510(k)

MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS

K-Number: K993234 · 1999-11-10

ApplicantMicromedics, Inc.
Decision Date1999-11-10
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 1999-11-10 under 510(k) number K993234. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS?

MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Micromedics, Inc.. The 510(k) number is K993234.

When did MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS receive FDA 510(k) clearance?

MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS received FDA 510(k) clearance on 1999-11-10, under 510(k) number K993234.

Who is the listed applicant for MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS?

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

What is the FDA product code for MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS?

The FDA product code for MICROMEDICS S&T PARTIAL OSSICULAR REPLACEMENT PROSTHESIS is ETB.

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Related Devices (Code: ETB)

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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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