TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG— 510(k) K810193

Name: FDA 510(k) clearance K810193
Creator: U.S. Food and Drug Administration
Published: 1981-03-20

Substantially Equivalent

Ace Orthopedic Manufacturing Co.

FDA 510(k) clearance K810193 for TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG, Substantially Equivalent on 1981-03-20. Applicant: Ace Orthopedic Manufacturing Co.. Device class: 2.

Clearance details

Applicant: Ace Orthopedic Manufacturing Co.
Product code: Code HAX
Device class: Class 2
Regulation: 21 CFR 882.5960
Advisory panel: Neurology
Date received: 1981-01-23
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K926047 — ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW1993-03-31
K920738 — ACE 100 DEGREES TUBULAR PLATE1992-07-27

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