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 Fastener, Fixation, Nondegradable, Soft Tissue
510(k) Number K240835
Device Name Suture Button Repair System
Applicant
Skeletal Dynamics, Inc.
7300 N. Kendall Dr.
Suite 800
Miami,  FL  33156
Applicant Contact Alexandra Rodriguez Rojas
Correspondent
Skeletal Dynamics, Inc.
7300 N. Kendall Dr.
Suite 800
Miami,  FL  33156
Correspondent Contact Alexandra Rodriguez Rojas
Regulation Number888.3040
Classification Product Code
MBI  
Date Received03/26/2024
Decision Date 07/19/2024
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
-
-