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FDA 510(k)

MAY HUMERUS PLATES

K-Number: K912936 · 1991-09-06

Decision Date1991-09-06
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MAY HUMERUS PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Turnkey Intergration USA, Inc.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K912936. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAY HUMERUS PLATES?

MAY HUMERUS PLATES is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Turnkey Intergration USA, Inc.. The 510(k) number is K912936.

When did MAY HUMERUS PLATES receive FDA 510(k) clearance?

MAY HUMERUS PLATES received FDA 510(k) clearance on 1991-09-06, under 510(k) number K912936.

Who is the listed applicant for MAY HUMERUS PLATES?

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

What is the FDA product code for MAY HUMERUS PLATES?

The FDA product code for MAY HUMERUS PLATES is HRS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Turnkey Intergration USA, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 26 devices →

Related Devices (Code: HRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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