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

Reliance Posterior Cervical-Thoracic System

K Number: K142867 · Decision Apr 29, 2015
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
24
Review Days
210

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Basic Information

Device Name
Reliance Posterior Cervical-Thoracic System
K Number
K142867
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Reliance Medical Systems, LLC
Date Received
October 1, 2014
Decision Date
April 29, 2015
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

Other 510(k) clearances with the same product code (KWP), 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
K183049 Reliance Lumbar IBF System
K173283 Reliance Lumbar IBF System
K173102 Reliance Cervical IBF System
K172489 Reliance Cervical IBF System
K162066 Reliance Spinal Screw System
K160463 Reliance Lumbar IBF System
K152131 Reliance Spinal Screw System
K142269 Reliance Cervical IBF System
Search all 24 clearances from Reliance Medical Systems, LLC →