ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002— 510(k) K903213

Name: FDA 510(k) clearance K903213
Creator: U.S. Food and Drug Administration
Published: 1990-07-27

Substantially Equivalent

Percutaneous Technologies

FDA 510(k) clearance K903213 for ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002, Substantially Equivalent on 1990-07-27. Applicant: Percutaneous Technologies. Device class: 2.

Clearance details

Applicant: Percutaneous Technologies
Product code: Code HEX
Device class: Class 2
Regulation: 21 CFR 884.1630
Advisory panel: Obstetrics/Gynecology
Date received: 1990-07-23
Decision date: 1990-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walnut, CA, US

Download summary PDF View on FDA.gov ↗

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