Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Scott Rucker
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230808
03/23/2023
PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System
Kyocera Medical Technologies, Inc.
K212980
09/17/2021
Tesera-k ALIF System
Kyocera Medical Technologies, Inc.
K223105
09/30/2022
Tesera-K SC System
Kyocera Medical Technologies, Inc.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact