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

MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEM

K Number: K132900 · Decision Oct 25, 2013
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
6
Review Days
39

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Basic Information

Device Name
MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEM
K Number
K132900
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intelligent Implant Systems, LLC
Date Received
September 16, 2013
Decision Date
October 25, 2013
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

Similar 510(k) Clearances

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Other Clearances by Intelligent Implant Systems, LLC

K Number Device Name
K173935 Mediant Anterior Cervical Plating System
K163056 Revolution™ Spinal Fixation System
K160216 Revolution Spinal Fixation System
K142939 Revolution Spinal Fixation System
K121682 ACTIVE SCREW BONE SCREW