FDA 510(k) Applications Submitted by ANDREW J ADAMS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K190055 |
01/11/2019 |
Duo Lumbar Interbody Fusion Device |
Spineology Inc. |
| K210155 |
01/21/2021 |
Duo Expandable Interbody Fusion System |
Spineology Inc. |
| DEN200010 |
02/19/2020 |
Spineology Interbody Fusion System |
Spineology, Inc. |
| K191091 |
04/24/2019 |
Rampart One Lumbar Interbody Fusion System |
Spineology, Inc. |
| K192047 |
07/31/2019 |
RampartÖ One Lumbar Interbody Fusion System |
Spineology, Inc. |
| K082987 |
10/07/2008 |
HRK-63-16 KNEE ARRAY COIL, HRK-127-16 KNEE ARRAY COIL |
INVIVO |
| K213876 |
12/13/2021 |
Spineology Navigation Instruments |
Spineology Inc. |
| K130678 |
03/13/2013 |
BIOMARC GOLD FIDUCIAL MARKER |
CARBON MEDICAL TECHNOLOGIES, INC. |
| K110772 |
03/21/2011 |
BIOMARC FIDUCIAL MARKER |
CARBON MEDICAL TECHNOLOGIES, INC. |
| K132064 |
07/03/2013 |
BIOMARC FIDUCIAL MARKER |
CARBON MEDICAL TECHNOLOGIES, INC. |
| K132708 |
08/29/2013 |
BIOMARC FIDUCIAL MARKER |
CARBON MEDICAL TECHNOLOGIES, INC. |
| K133148 |
10/17/2013 |
BIOMARC COAXIAL NEEDLE |
CARBON MEDICAL TECHNOLOGIES, INC. |
| K172227 |
07/25/2017 |
Endoscopic Injection Needle |
Carbon Medical Technologies, Inc. |
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