BONESOURCE HAC— 510(k) K021440

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K021440 for BONESOURCE HAC, Substantially Equivalent on 2002-08-02. Applicant: Stryker Instruments. Device class: 2.

Clearance details

Applicant: Stryker Instruments
Product code: Code GXP
Device class: Class 2
Regulation: 21 CFR 882.5300
Advisory panel: Neurology
Date received: 2002-05-06
Decision date: 2002-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, 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.