MODIFICATION TO CRANIOPLASTIC, MODEL 43-1280— 510(k) K071791

Substantially Equivalent

Codman & Shurtleff, Inc.

FDA 510(k) clearance K071791 for MODIFICATION TO CRANIOPLASTIC, MODEL 43-1280, Substantially Equivalent on 2007-07-30. Applicant: Codman & Shurtleff, Inc..

Clearance details

Applicant: Codman & Shurtleff, Inc.
Product code: Code GXP
Advisory panel: Neurology
Date received: 2007-07-02
Decision date: 2007-07-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Raynham, MA, US

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