FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

Proficient (TM) Facet Screw Spine System

K Number: K142980 · Decision Jan 16, 2015
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
59
Review Days
93

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
Proficient (TM) Facet Screw Spine System
K Number
K142980
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Wave, Inc.
Date Received
October 15, 2014
Decision Date
January 16, 2015
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

Similar 510(k) Clearances

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

View all

Other Clearances by Spine Wave, Inc.

K Number Device Name
K260286 Dynamo™ Spinal Cement; Salvo® Spine System
K261159 Exceed® Biplanar Expandable Interbody System
K243816 Testa TP Pivoting Spacer System
K251131 Annex® 2 Adjacent Level System
K243514 Salvo® Robotic Navigation Instruments
K240685 Salvo® Spine System
K231275 Exceed™ Biplanar Expandable Interbody System
K222362 Salvo® Spine System
K202476 Salvo® Spine System
K192526 Spine Wave Navigated Instruments
Search all 59 clearances from Spine Wave, Inc. →