FDA 510(k) Applications Submitted by Providence Medical Technology, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K180876 |
04/03/2018 |
DTRAX Spinal System |
Providence Medical Technology, Inc. |
| K172279 |
07/28/2017 |
PMT Posterior Fixation System |
Providence Medical Technology, Inc. |
| K212636 |
08/19/2021 |
CORUS Spinal System-X |
Providence Medical Technology, Inc. |
| K122801 |
09/13/2012 |
PROVIDENCE CERVICAL CAGE |
PROVIDENCE MEDICAL TECHNOLOGY, INC. |
| K163474 |
12/12/2016 |
CAVUX CervicalCage-L SA System |
PROVIDENCE MEDICAL TECHNOLOGY, INC. |
| K183589 |
12/21/2018 |
PMT Facet Screw |
Providence Medical Technology, Inc. |
| K121713 |
06/11/2012 |
PMT BONE SCREWS |
PROVIDENCE MEDICAL TECHNOLOGY, INC. |
| K190201 |
02/04/2019 |
CORUS Spinal System |
Providence Medical Technology, Inc. |
| K170698 |
03/07/2017 |
ALLY(TM) Bone Screws |
Providence Medical Technology, Inc. |
| K163374 |
12/01/2016 |
ALLYÖ Facet Screws |
PROVIDENCE MEDICAL TECHNOLOGY, INC. |
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