CODMAN SURGICAL PATTIE

Neurosurgical Paddie

Codman & Shurtleff, Inc.

The following data is part of a premarket notification filed by Codman & Shurtleff, Inc. with the FDA for Codman Surgical Pattie.

Pre-market Notification Details

• Device ID: K880402
• 510k Number: K880402
• Device Name: CODMAN SURGICAL PATTIE
• Classification: Neurosurgical Paddie
• Applicant: Codman & Shurtleff, Inc. 41 PACELLA PARK DR. RANDOLPH INDUSTRIAL PARK Randolph, MA 02368 -1794
• Contact: Thomas J Courage
• Correspondent: Thomas J Courage; Codman & Shurtleff, Inc. 41 PACELLA PARK DR. RANDOLPH INDUSTRIAL PARK Randolph, MA 02368 -1794
• Product Code: HBA
• CFR Regulation Number: 882.4700 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1988-01-29
• Decision Date: 1988-03-02

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00381780513356	K880402	000
00381780515022	K880402	000
00381780515015	K880402	000
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