SCHOLTEN FRAME— 510(k) K900405

Name: FDA 510(k) clearance K900405
Creator: U.S. Food and Drug Administration
Published: 1990-03-01

Substantially Equivalent

Scholten Surgical Instruments, Inc.

FDA 510(k) clearance K900405 for SCHOLTEN FRAME, Substantially Equivalent on 1990-03-01. Applicant: Scholten Surgical Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Scholten Surgical Instruments, Inc.
Product code: Code JEB
Device class: Class 1
Regulation: 21 CFR 878.4950
Advisory panel: General, Plastic Surgery
Date received: 1990-01-29
Decision date: 1990-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, CA, US

Download summary PDF View on FDA.gov ↗

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