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FDA 510(k)

SHOULDER NAIL PLATE

K-Number: K052294 · 2005-10-21

Decision Date2005-10-21
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SHOULDER NAIL PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Hand Innovations, LLC. It received FDA 510(k) clearance on 2005-10-21 under 510(k) number K052294. 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 SHOULDER NAIL PLATE?

SHOULDER NAIL PLATE is a medical device that received FDA 510(k) clearance on 2005-10-21. The listed applicant is Hand Innovations, LLC. The 510(k) number is K052294.

When did SHOULDER NAIL PLATE receive FDA 510(k) clearance?

SHOULDER NAIL PLATE received FDA 510(k) clearance on 2005-10-21, under 510(k) number K052294.

Who is the listed applicant for SHOULDER NAIL PLATE?

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

What is the FDA product code for SHOULDER NAIL PLATE?

The FDA product code for SHOULDER NAIL PLATE 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 Hand Innovations, LLC 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 7 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

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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