CARBIDE CUTTING INSTRUMENT/INTRAARTICU— 510(k) K802598

Name: FDA 510(k) clearance K802598
Creator: U.S. Food and Drug Administration
Published: 1980-11-19

Substantially Equivalent

The Anspach Effort, Inc.

FDA 510(k) clearance K802598 for CARBIDE CUTTING INSTRUMENT/INTRAARTICU, Substantially Equivalent on 1980-11-19. Applicant: The Anspach Effort, Inc.. Device class: 1.

Clearance details

Applicant: The Anspach Effort, Inc.
Product code: Code HTT
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1980-10-21
Decision date: 1980-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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