JOHNSON AND JOHNSON POWER SYSTEM— 510(k) K913629

Name: FDA 510(k) clearance K913629
Creator: U.S. Food and Drug Administration
Published: 1991-11-13

Substantially Equivalent

Johnson & Johnson Orthopaedics, Inc.

FDA 510(k) clearance K913629 for JOHNSON AND JOHNSON POWER SYSTEM, Substantially Equivalent on 1991-11-13. Applicant: Johnson & Johnson Orthopaedics, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Orthopaedics, Inc.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1991-08-15
Decision date: 1991-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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