SMARTJET BONE GRAFT LIQUID APPLICATOR (SPRAY TIP), MODEL SK/S, SMARTJET BONE GRAFT LIQUID APPLICATOR (DUAL LUMEN CANNULA— 510(k) K011032

Name: FDA 510(k) clearance K011032
Creator: U.S. Food and Drug Administration
Published: 2001-07-03

Substantially Equivalent

Harvest Technologies, Corp.

FDA 510(k) clearance K011032 for SMARTJET BONE GRAFT LIQUID APPLICATOR (SPRAY TIP), MODEL SK/S, SMARTJET BONE GRAFT LIQUID APPLICATOR (DUAL LUMEN CANNULA, Substantially Equivalent on 2001-07-03. Applicant: Harvest Technologies, Corp.. Device class: 2.

Clearance details

Applicant: Harvest Technologies, Corp.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2001-04-05
Decision date: 2001-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plymouth, MA, US

Download summary PDF View on FDA.gov ↗

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