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FDA 510(k)

RESORBABLE HAMMERTOE PIN

K-Number: K011137 · 2001-06-19

ApplicantBiomet, Inc.
Decision Date2001-06-19
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RESORBABLE HAMMERTOE 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 2001-06-19 under 510(k) number K011137. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESORBABLE HAMMERTOE PIN?

RESORBABLE HAMMERTOE PIN is a medical device that received FDA 510(k) clearance on 2001-06-19. The listed applicant is Biomet, Inc.. The 510(k) number is K011137.

When did RESORBABLE HAMMERTOE PIN receive FDA 510(k) clearance?

RESORBABLE HAMMERTOE PIN received FDA 510(k) clearance on 2001-06-19, under 510(k) number K011137.

Who is the listed applicant for RESORBABLE HAMMERTOE 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 RESORBABLE HAMMERTOE PIN?

The FDA product code for RESORBABLE HAMMERTOE PIN is JDW.

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: JDW)

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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