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FDA 510(k)

HAMMER TOE IMPLANT

K-Number: K122959 · 2012-11-07

Decision Date2012-11-07
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HAMMER TOE IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Trilliant Surgical, Ltd.. It received FDA 510(k) clearance on 2012-11-07 under 510(k) number K122959. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAMMER TOE IMPLANT?

HAMMER TOE IMPLANT is a medical device that received FDA 510(k) clearance on 2012-11-07. The listed applicant is Trilliant Surgical, Ltd.. The 510(k) number is K122959.

When did HAMMER TOE IMPLANT receive FDA 510(k) clearance?

HAMMER TOE IMPLANT received FDA 510(k) clearance on 2012-11-07, under 510(k) number K122959.

Who is the listed applicant for HAMMER TOE IMPLANT?

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

What is the FDA product code for HAMMER TOE IMPLANT?

The FDA product code for HAMMER TOE IMPLANT is HWC. This falls under the Cardiovascular category.

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 Trilliant Surgical, Ltd. 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 14 devices →

Related Devices (Code: HWC)

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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