HARRIS CEMENT RESTRICTOR— 510(k) K810353

Name: FDA 510(k) clearance K810353
Creator: U.S. Food and Drug Administration
Published: 1981-02-23

Substantially Equivalent

Cintor Orthopaedic Div.

FDA 510(k) clearance K810353 for HARRIS CEMENT RESTRICTOR, Substantially Equivalent on 1981-02-23. Applicant: Cintor Orthopaedic Div.. Device class: 2.

Clearance details

Applicant: Cintor Orthopaedic Div.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1981-02-10
Decision date: 1981-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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