STRYKER ORAL MAX SYSTEM— 510(k) K954690

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K954690 for STRYKER ORAL MAX SYSTEM, Substantially Equivalent on 1996-08-20. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 1995-10-11
Decision date: 1996-08-20
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.