Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Intervertebral Fusion Device With Integrated Fixation, Lumbar
510(k) Number K241321
Device Name Juliet® Ti LL Lumbar Interbody Device
Applicant
Spineart SA
3 Chemin Du Pré-Fleuri
Plan Les Ouates,  CH 1228
Applicant Contact Estelle Lefeuvre
Correspondent
Spineart SA
3 Chemin Du Pré-Fleuri
Plan Les Ouates,  CH 1228
Correspondent Contact Estelle Lefeuvre
Regulation Number888.3080
Classification Product Code
OVD  
Subsequent Product Code
MAX  
Date Received05/10/2024
Decision Date 07/18/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-