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

Arsenal Spinal Fixation System

K Number: K152968 · Decision Dec 30, 2015
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
93
Review Days
83

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Basic Information

Device Name
Arsenal Spinal Fixation System
K Number
K152968
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alphatec Spine, Inc.
Date Received
October 8, 2015
Decision Date
December 30, 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

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Other Clearances by Alphatec Spine, Inc.

K Number Device Name
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K251965 Proximity Anterior Cervical Plate System; Segmental Plating System (SPS)
K251080 IdentiTi II Cervical Interbody System
K243461 Calibrate Interbody Systems
K242364 IdentiTi™ II Interbody System
K242147 Calibrate LTX Interbody System; Calibrate NanoTec LTX Interbody System
K241519 Invictus® Small Stature Spinal Fixation System
K240199 IntraOp Alignment System
Search all 93 clearances from Alphatec Spine, Inc. →