INVUITY BRITEFIELD MCCULLOCH RETRACTOR SYSTEM— 510(k) K090070

Name: FDA 510(k) clearance K090070
Creator: U.S. Food and Drug Administration
Published: 2009-04-22

Substantially Equivalent

Invuity, Inc.

FDA 510(k) clearance K090070 for INVUITY BRITEFIELD MCCULLOCH RETRACTOR SYSTEM, Substantially Equivalent on 2009-04-22. Applicant: Invuity, Inc.. Device class: 2.

Clearance details

Applicant: Invuity, Inc.
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2009-01-12
Decision date: 2009-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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