MODIFIED SAW BLADES TO THE SAGITAL SAW— 510(k) K884839

Name: FDA 510(k) clearance K884839
Creator: U.S. Food and Drug Administration
Published: 1988-12-07

Substantially Equivalent

Dyonics, Inc.

FDA 510(k) clearance K884839 for MODIFIED SAW BLADES TO THE SAGITAL SAW, Substantially Equivalent on 1988-12-07. Applicant: Dyonics, Inc.. Device class: 1.

Clearance details

Applicant: Dyonics, Inc.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1988-11-21
Decision date: 1988-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

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