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FDA 510(k)

FIXATION (STEINMANN) PINS

K-Number: K013888 · 2002-05-01

ApplicantMiltex, Inc.
Decision Date2002-05-01
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FIXATION (STEINMANN) PINS is the device name listed in this FDA 510(k) record. The listed applicant is Miltex, Inc.. It received FDA 510(k) clearance on 2002-05-01 under 510(k) number K013888. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIXATION (STEINMANN) PINS?

FIXATION (STEINMANN) PINS is a medical device that received FDA 510(k) clearance on 2002-05-01. The listed applicant is Miltex, Inc.. The 510(k) number is K013888.

When did FIXATION (STEINMANN) PINS receive FDA 510(k) clearance?

FIXATION (STEINMANN) PINS received FDA 510(k) clearance on 2002-05-01, under 510(k) number K013888.

Who is the listed applicant for FIXATION (STEINMANN) PINS?

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

What is the FDA product code for FIXATION (STEINMANN) PINS?

The FDA product code for FIXATION (STEINMANN) PINS is HTY.

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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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