EXTERNAL ARTICULATION— 510(k) K781840

Name: FDA 510(k) clearance K781840
Creator: U.S. Food and Drug Administration
Published: 1978-11-08

Substantially Equivalent

Ace Orthopedic Manufacturing Co.

FDA 510(k) clearance K781840 for EXTERNAL ARTICULATION, Substantially Equivalent on 1978-11-08. Applicant: Ace Orthopedic Manufacturing Co.. Device class: 2.

Clearance details

Applicant: Ace Orthopedic Manufacturing Co.
Product code: Code JEC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1978-10-27
Decision date: 1978-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.