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FDA 510(k)

SHORT AND LONG SOFT TISSUE ATTACHMENT

K-Number: K022079 · 2002-09-24

ApplicantBiomet, Inc.
Decision Date2002-09-24
Product CodeKWT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SHORT AND LONG SOFT TISSUE ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2002-09-24 under 510(k) number K022079. The device is classified under product code KWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHORT AND LONG SOFT TISSUE ATTACHMENT?

SHORT AND LONG SOFT TISSUE ATTACHMENT is a medical device that received FDA 510(k) clearance on 2002-09-24. The listed applicant is Biomet, Inc.. The 510(k) number is K022079.

When did SHORT AND LONG SOFT TISSUE ATTACHMENT receive FDA 510(k) clearance?

SHORT AND LONG SOFT TISSUE ATTACHMENT received FDA 510(k) clearance on 2002-09-24, under 510(k) number K022079.

Who is the listed applicant for SHORT AND LONG SOFT TISSUE ATTACHMENT?

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 SHORT AND LONG SOFT TISSUE ATTACHMENT?

The FDA product code for SHORT AND LONG SOFT TISSUE ATTACHMENT is KWT.

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.

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Related Devices (Code: KWT)

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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