OSTEO-CABLE SLEEVE— 510(k) K024022

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K024022 for OSTEO-CABLE SLEEVE, Substantially Equivalent on 2003-01-23. Applicant: Biomet, Inc.. Device class: 1.

Clearance details

Applicant: Biomet, Inc.
Product code: Code HXN
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 2002-12-05
Decision date: 2003-01-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.