STRYKER TOTAL PERFORMANCE (TPS) SYSTEM— 510(k) K032117

Name: FDA 510(k) clearance K032117
Creator: U.S. Food and Drug Administration
Published: 2003-08-08

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K032117 for STRYKER TOTAL PERFORMANCE (TPS) SYSTEM, Substantially Equivalent on 2003-08-08. Applicant: Stryker Instruments. Device class: 2.

Clearance details

Applicant: Stryker Instruments
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2003-07-09
Decision date: 2003-08-08
Decision: Substantially Equivalent
Clearance type: Special
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.