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
-
1 to 10 of 16 Results
ProductCode: KWS Applicant: BIOMET MANUFACTURING CORP. Decision Date To: 05/07/2024
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 16 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
comprehensive® shoulder system, comprehensive® reverse shoulder system Biomet Manufacturing Corp. K214001 03/15/2023
comprehensive® convertible glenoid - vivacit-e liner Biomet Manufacturing Corp. K211729 11/04/2021
comprehensive shoulder system Biomet Manufacturing Corp. K193038 10/28/2020
comprehensive segmental revision system (srs) Biomet Manufacturing Corp. K173411 02/08/2018
comprehensive srs/nexel elbow BIOMET MANUFACTURING CORP. K153398 02/03/2016
titanium versa-dial humeral head prosthesis BIOMET MANUFACTURING CORP. K140390 09/10/2014
porous coated comprehensive fracture stems BIOMET MANUFACTURING CORP. K140652 07/03/2014
biomet stage one disposable cement spacer molds for temporary hemi-shoulder prosthesis BIOMET MANUFACTURING CORP. K131135 01/22/2014
comprehensive reverse shoulder - titanium glenosphere BIOMET MANUFACTURING CORP. K131353 10/08/2013
comprehensive reverse shoulder screws BIOMET MANUFACTURING CORP. K132239 09/06/2013
-
-