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

PRECICE Plating System

K Number: K192181 · Decision Nov 7, 2019
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
19
Review Days
87

Basic Information

Device Name
PRECICE Plating System
K Number
K192181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NuVasive Specialized Orthopedics, Inc.
Date Received
August 12, 2019
Decision Date
November 7, 2019
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Similar 510(k) Clearances

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

View all

Other Clearances by NuVasive Specialized Orthopedics, Inc.

K Number Device Name
K230765 Precice Ankle Salvage System
K220234 Precice Intramedullary Limb Lengthening System
K202348 External Remote Controller ERC 4P
K200430 Precice® Ankle Salvage System
K201567 Precice® Bone Transport System
K201543 MAGEC® System
K193617 Precice® Screws
K193016 PRECICE Bone Transport System
K191336 PRECICE System
K182170 PRECICE® BONE TRANSPORT™ System
Search all 19 clearances from NuVasive Specialized Orthopedics, Inc. →