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FDA 510(k)

STARR FRAME STEINMANN PIN

K-Number: K082017 · 2008-10-10

ApplicantStarr Frame, LLC
Decision Date2008-10-10
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STARR FRAME STEINMANN PIN is the device name listed in this FDA 510(k) record. The listed applicant is Starr Frame, LLC. It received FDA 510(k) clearance on 2008-10-10 under 510(k) number K082017. 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 STARR FRAME STEINMANN PIN?

STARR FRAME STEINMANN PIN is a medical device that received FDA 510(k) clearance on 2008-10-10. The listed applicant is Starr Frame, LLC. The 510(k) number is K082017.

When did STARR FRAME STEINMANN PIN receive FDA 510(k) clearance?

STARR FRAME STEINMANN PIN received FDA 510(k) clearance on 2008-10-10, under 510(k) number K082017.

Who is the listed applicant for STARR FRAME STEINMANN PIN?

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

What is the FDA product code for STARR FRAME STEINMANN PIN?

The FDA product code for STARR FRAME STEINMANN PIN is HTY.

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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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