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

Reliance Spinal Screw System

K Number: K162066 · Decision Dec 2, 2016
Classifications
1
FEI Numbers
338
Registration Numbers
338
Same Product Code
308
Applicant Total
23
Review Days
129

Basic Information

Device Name
Reliance Spinal Screw System
K Number
K162066
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Reliance Medical Systems, LLC
Date Received
July 26, 2016
Decision Date
December 2, 2016
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

Similar 510(k) Clearances

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

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Other Clearances by Reliance Medical Systems, LLC

K Number Device Name
K202266 Reliance Cervical IBF System
K210874 Reliance Spinal Screw System
K173283 Reliance Lumbar IBF System
K173102 Reliance Cervical IBF System
K172489 Reliance Cervical IBF System
K160463 Reliance Lumbar IBF System
K152131 Reliance Spinal Screw System
K142269 Reliance Cervical IBF System
K142867 Reliance Posterior Cervical-Thoracic System
K142217 Reliance Interspinous Plate System
Search all 23 clearances from Reliance Medical Systems, LLC →