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

KLS Martin Cannulated Headless Screws

K Number: K161259 · Decision Dec 19, 2016
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
20
Review Days
229

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Basic Information

Device Name
KLS Martin Cannulated Headless Screws
K Number
K161259
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KLS Martin L.P.
Date Received
May 4, 2016
Decision Date
December 19, 2016
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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Other Clearances by KLS Martin L.P.

K Number Device Name
K254162 KLS Martin Ixos System
K250620 KLS Martin Ixos System
K221938 KLS Martin Pure Pectus System
K220050 KLS Martin IPS Distraction
K173320 KLS Martin L1 MMF System
K163579 KLS Martin Individual Patient Solutions
K163315 Internal Distraction - Sterile
K170124 Level One Hand Plating System
K161470 Internal Distraction - Sterile
K151983 KLS Martin LSS Plating System
Search all 20 clearances from KLS Martin L.P. →