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FDA 510(k)

SMALL HAMMER TOE PIN

K-Number: K021828 · 2002-07-01

ApplicantBiomet, Inc.
Decision Date2002-07-01
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMALL HAMMER TOE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2002-07-01 under 510(k) number K021828. 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 SMALL HAMMER TOE PIN?

SMALL HAMMER TOE PIN is a medical device that received FDA 510(k) clearance on 2002-07-01. The listed applicant is Biomet, Inc.. The 510(k) number is K021828.

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

SMALL HAMMER TOE PIN received FDA 510(k) clearance on 2002-07-01, under 510(k) number K021828.

Who is the listed applicant for SMALL HAMMER TOE PIN?

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

What is the FDA product code for SMALL HAMMER TOE PIN?

The FDA product code for SMALL HAMMER TOE PIN 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 Biomet, 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 418 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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