STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM— 510(k) K991696

Name: FDA 510(k) clearance K991696
Creator: U.S. Food and Drug Administration
Published: 1999-10-25

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K991696 for STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM, Substantially Equivalent on 1999-10-25. 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: 1999-05-18
Decision date: 1999-10-25
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.