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FDA 510(k) Applications Submitted by RELIANCE MEDICAL SYSTEMS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K101112
04/21/2010
RELIANCE SPINAL SCREW SYSTEM
RELIANCE MEDICAL SYSTEMS
K180687
03/15/2018
Reliance Lumber IBF System
Reliance Medical Systems
K181118
04/27/2018
Reliance Lumbar IBF System
Reliance Medical Systems
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