CEBOTOME DRILL

Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment

AMERICAN STERILIZER CO.

The following data is part of a premarket notification filed by American Sterilizer Co. with the FDA for Cebotome Drill.

Pre-market Notification Details

• Device ID: K800275
• 510k Number: K800275
• Device Name: CEBOTOME DRILL
• Classification: Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment
• Applicant: AMERICAN STERILIZER CO. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: HSZ
• CFR Regulation Number: 878.4820 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1980-02-07
• Decision Date: 1980-02-19

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10845854023402	K800275	000