FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

IMPLANET Spine System (ISS)

K Number: K143731 · Decision Apr 14, 2015
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
15
Review Days
106

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
IMPLANET Spine System (ISS)
K Number
K143731
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implanet, S.A.
Date Received
December 29, 2014
Decision Date
April 14, 2015
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 Implanet, S.A.

K Number Device Name
K230026 SQUALE
K192084 Madison Total Knee System
K191217 JAZZ PF
K182771 ISS-JAZZ Screw System and JAZZ CAP SP
K171881 JAZZ Passer Band
K170730 JAZZ System, including JAZZ Band
K162764 JAZZ FRAME SYSTEM
K160226 JAZZ CLAW System (hooks and rods) and JAZZ CLAW connector
K153348 JAZZ LOCK
K151740 JAZZ System
Search all 15 clearances from Implanet, S.A. →