SPECIALIST(R) WALKER— 510(k) K924984

Name: FDA 510(k) clearance K924984
Creator: U.S. Food and Drug Administration
Published: 1993-02-01

Substantially Equivalent

Johnson & Johnson Orthopaedics, Inc.

FDA 510(k) clearance K924984 for SPECIALIST(R) WALKER, Substantially Equivalent on 1993-02-01. Applicant: Johnson & Johnson Orthopaedics, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Orthopaedics, Inc.
Product code: Code FYH
Device class: Class 1
Regulation: 21 CFR 878.3910
Advisory panel: General, Plastic Surgery
Date received: 1992-10-01
Decision date: 1993-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

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