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

DRIVER/EXTRACTOR

K Number: K903257 · Decision Jul 30, 1990
Classifications
1
FEI Numbers
1140
Registration Numbers
1140
Same Product Code
57
Applicant Total
47
Review Days
6

Basic Information

Device Name
DRIVER/EXTRACTOR
K Number
K903257
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
ONYX MEDICAL CORP.
Date Received
July 24, 1990
Decision Date
July 30, 1990
Product Code
LXH
Advisory Committee
Orthopedic
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
LXH Orthopedic Manual Surgical Instrument

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