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

Headless Compression Screw System

K Number: K143624 · Decision Jan 13, 2015
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
18
Review Days
22

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Basic Information

Device Name
Headless Compression Screw System
K Number
K143624
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Skeletal Dynamics, LLC
Date Received
December 22, 2014
Decision Date
January 13, 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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