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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