FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ETHICON DRILL BIT AND DRILL GUIDE

K Number: K944590 · Decision May 11, 1995
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
55
Applicant Total
172
Review Days
234

Basic Information

Device Name
ETHICON DRILL BIT AND DRILL GUIDE
K Number
K944590
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ETHICON, INC.
Date Received
September 19, 1994
Decision Date
May 11, 1995
Product Code
HSZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment

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