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

CancelleX Porous Titanium Lumbar Interbody Device

K Number: K190364 · Decision Apr 18, 2019
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
16
Review Days
62

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Basic Information

Device Name
CancelleX Porous Titanium Lumbar Interbody Device
K Number
K190364
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xenco Medical, LLC
Date Received
February 15, 2019
Decision Date
April 18, 2019
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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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
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
K160986 Xenco Medical Pedicle Screw System
Search all 16 clearances from Xenco Medical, LLC →