GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM— 510(k) K935757

Name: FDA 510(k) clearance K935757
Creator: U.S. Food and Drug Administration
Published: 1994-04-15

Substantially Equivalent

Greenleaf Medical Systems, Inc.

FDA 510(k) clearance K935757 for GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM, Substantially Equivalent on 1994-04-15. Applicant: Greenleaf Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Greenleaf Medical Systems, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1993-11-26
Decision date: 1994-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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