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FDA 510(k)

AOS PROXIMAL HUMERAL NAIL

K-Number: K090478 · 2009-03-26

ApplicantAdvanced Orthopaedic Solutions, Inc.
Decision Date2009-03-26
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AOS PROXIMAL HUMERAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Orthopaedic Solutions, Inc.. It received FDA 510(k) clearance on 2009-03-26 under 510(k) number K090478. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOS PROXIMAL HUMERAL NAIL?

AOS PROXIMAL HUMERAL NAIL is a medical device that received FDA 510(k) clearance on 2009-03-26. The listed applicant is Advanced Orthopaedic Solutions, Inc.. The 510(k) number is K090478.

When did AOS PROXIMAL HUMERAL NAIL receive FDA 510(k) clearance?

AOS PROXIMAL HUMERAL NAIL received FDA 510(k) clearance on 2009-03-26, under 510(k) number K090478.

Who is the listed applicant for AOS PROXIMAL HUMERAL NAIL?

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

What is the FDA product code for AOS PROXIMAL HUMERAL NAIL?

The FDA product code for AOS PROXIMAL HUMERAL NAIL is HSB.

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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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