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

RELIANCE SPINAL SCREW SYSTEM

K Number: K081978 · Decision Mar 26, 2009
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
24
Review Days
258

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Basic Information

Device Name
RELIANCE SPINAL SCREW SYSTEM
K Number
K081978
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 11, 2008
Decision Date
March 26, 2009
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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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 →