RUBIN BONE PLANER W/REPLACEABLE BLADE— 510(k) K884473

Name: FDA 510(k) clearance K884473
Creator: U.S. Food and Drug Administration
Published: 1988-12-09

Substantially Equivalent

Neo Contemporary Co.

FDA 510(k) clearance K884473 for RUBIN BONE PLANER W/REPLACEABLE BLADE, Substantially Equivalent on 1988-12-09. Applicant: Neo Contemporary Co.. Device class: 1.

Clearance details

Applicant: Neo Contemporary Co.
Product code: Code GAC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-10-25
Decision date: 1988-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Quincy, MA, US

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