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

Momentum™ Posterior Spinal Fixation System

K Number: K191932 · Decision Oct 2, 2019
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
8
Review Days
75

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Basic Information

Device Name
Momentum™ Posterior Spinal Fixation System
K Number
K191932
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ulrich Medical USA
Date Received
July 19, 2019
Decision Date
October 2, 2019
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.

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Other Clearances by Ulrich Medical USA

K Number Device Name
K231809 Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement; Momentum® MIS Posterior Spinal Fixation System with G21 V-STEADY Bone Cement
K230614 Cortium™
K223274 Momentum® MIS Posterior Spinal Fixation System
K220696 uCerv Flux-C 3D Porous Titanium Cervical Interbody
K200845 Navigation Module of the Momentum System
K181921 Solidity Vertebral Body Replacement
K150666 uNion Cervical Plate System