OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION)— 510(k) K881060

Name: FDA 510(k) clearance K881060
Creator: U.S. Food and Drug Administration
Published: 1988-03-25

Substantially Equivalent

Orthopedic Systems, Inc.

FDA 510(k) clearance K881060 for OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION), Substantially Equivalent on 1988-03-25. Applicant: Orthopedic Systems, Inc.. Device class: 1.

Clearance details

Applicant: Orthopedic Systems, Inc.
Product code: Code JEA
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1988-03-04
Decision date: 1988-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hayward, CA, US

Download summary PDF View on FDA.gov ↗

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