FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ORTHOPEDIC SCREW SYSTEM

K Number: K972217 · Decision Nov 20, 1997
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
57
Review Days
161

Basic Information

Device Name
ORTHOPEDIC SCREW SYSTEM
K Number
K972217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ferguson Medical
Date Received
June 12, 1997
Decision Date
November 20, 1997
Product Code
HWC
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
HWC Screw, Fixation, Bone

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