LAMINECTOMY RONGEUR— 510(k) K901372

Substantially Equivalent

Zeppelin GmbH

FDA 510(k) clearance K901372 for LAMINECTOMY RONGEUR, Substantially Equivalent on 1990-06-28. Applicant: Zeppelin GmbH. Device class: 2.

Clearance details

Applicant: Zeppelin GmbH
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 1990-03-22
Decision date: 1990-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Germany, DE

Download summary PDF View on FDA.gov ↗

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