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FDA 510(k)

REPROCESSED PINS

K-Number: K100707 · 2010-06-25

ApplicantSterilmed, Inc.
Decision Date2010-06-25
Product CodeNDM
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REPROCESSED PINS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2010-06-25 under 510(k) number K100707. The device is classified under product code NDM. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED PINS?

REPROCESSED PINS is a medical device that received FDA 510(k) clearance on 2010-06-25. The listed applicant is Sterilmed, Inc.. The 510(k) number is K100707.

When did REPROCESSED PINS receive FDA 510(k) clearance?

REPROCESSED PINS received FDA 510(k) clearance on 2010-06-25, under 510(k) number K100707.

Who is the listed applicant for REPROCESSED PINS?

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

What is the FDA product code for REPROCESSED PINS?

The FDA product code for REPROCESSED PINS is NDM.

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Other records listing Sterilmed, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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