BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM— 510(k) K894184

Name: FDA 510(k) clearance K894184
Creator: U.S. Food and Drug Administration
Published: 1990-04-25

Substantially Equivalent for Some Indications

Biedermann Motech GmbH

FDA 510(k) clearance K894184 for BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM, Substantially Equivalent for Some Indications on 1990-04-25. Applicant: Biedermann Motech GmbH. Device class: 2.

Clearance details

Applicant: Biedermann Motech GmbH
Product code: Code JDN
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 1989-06-16
Decision date: 1990-04-25
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Vs-Schwenningen, DE

Download summary PDF View on FDA.gov ↗

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