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

Xenco Medical Pedicle Screw System

K Number: K160986 · Decision May 4, 2016
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
16
Review Days
26

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Xenco Medical Pedicle Screw System
K Number
K160986
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Xenco Medical, LLC
Date Received
April 8, 2016
Decision Date
May 4, 2016
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NKB), ordered by most recent decision date.

View all

Other Clearances by Xenco Medical, LLC

K Number Device Name
K243673 Xenco Medical CancelleX Cervical Interbody System
K223059 Xenco Medical InterAlign Cervical Interbody System
K213456 Xenco Medical Multilevel CerviKit
K191074 Sorrento Bone Graft Substitute
K190364 CancelleX Porous Titanium Lumbar Interbody Device
K173933 Sorrento Bioglass Bone Graft Substitute
K180373 CancelleX Porous Titanium Lumbar Interbody Device
K170611 SETx Pedicle Screw System
K160313 Xenco Medical Cervical Interbody System
K161478 Xenco Medical Posterior Cervical System
Search all 16 clearances from Xenco Medical, LLC →