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 prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
510(k) Number K110533
Device Name STRYKER PATIENT SPECIFIC CUTTING GUIDE
Applicant
STRYKER CORP.
325 Corporate Drive
Mahwah,  NJ  07430
Applicant Contact KAREN ARIEMMA
Correspondent
STRYKER CORP.
325 Corporate Drive
Mahwah,  NJ  07430
Correspondent Contact KAREN ARIEMMA
Regulation Number888.3565
Classification Product Code
MBH  
Subsequent Product Codes
JWH   OOG  
Date Received02/24/2011
Decision Date 05/19/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-