INTERVERTEBRAL DISC RONGEUR— 510(k) K903151

Substantially Equivalent

Von Zeppelin GmbH

FDA 510(k) clearance K903151 for INTERVERTEBRAL DISC RONGEUR, Substantially Equivalent on 1990-12-11. Applicant: Von Zeppelin GmbH. Device class: 2.

Clearance details

Applicant: Von Zeppelin GmbH
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 1990-07-18
Decision date: 1990-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pullach, 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.