Device Classification Name |
Orthosis, Spine, Plate, Laminoplasty, Metal
More FDA Info for this Device |
510(K) Number |
K231232 |
Device Name |
Orthosis, Spine, Plate, Laminoplasty, Metal |
Applicant |
Curiteva, Inc.
25127 Will McComb Drive
Tanner, AL 35671 US
Other 510(k) Applications for this Company
|
Contact |
Eric Linder
Other 510(k) Applications for this Contact |
Regulation Number |
888.3050
More FDA Info for this Regulation Number |
Classification Product Code |
NQW
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
04/28/2023 |
Decision Date |
06/28/2023 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|