FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

SELF- COMPRESSIVE SCREW

K Number: K153182 · Decision Nov 25, 2015
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
6
Review Days
22

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Basic Information

Device Name
SELF- COMPRESSIVE SCREW
K Number
K153182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neosteo
Date Received
November 3, 2015
Decision Date
November 25, 2015
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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K131471 SELF-COMPRESSIVE SCREW