Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Renovis Surgical Technologies Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180502
02/26/2018
S128 Anterior Lumbar Interbody Fusion (ALIF) System
Renovis Surgical Technologies Inc.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact