SILICONE BRAIN SPATULA SET— 510(k) K923723

Name: FDA 510(k) clearance K923723
Creator: U.S. Food and Drug Administration
Published: 1992-08-12

Substantially Equivalent

Redmond Neurosurgical, Inc.

FDA 510(k) clearance K923723 for SILICONE BRAIN SPATULA SET, Substantially Equivalent on 1992-08-12. Applicant: Redmond Neurosurgical, Inc.. Device class: 1.

Clearance details

Applicant: Redmond Neurosurgical, Inc.
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1992-07-27
Decision date: 1992-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Zurich, IL, US

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