Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by L & K Biomed Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231839
06/22/2023
CastleLoc-P Anterior Cervical Plate System, AccelFix Lumbar Plate System
L & K Biomed Co., Ltd.
K231840
06/22/2023
CastleLoc-S Posterior Cervical Fixation System
L & K Biomed Co., Ltd.
K231841
06/22/2023
PathLoc SI Joint Fusion System
L & K Biomed Co., Ltd.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact