• 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 plate, cranioplasty, preformed, non-alterable
510(k) Number K180513
Device Name CustomizedBone Service
Applicant
Fin-Ceramica Faenza S.p.A
via Ravegnana 186
Faenza,  IT 48018
Applicant Contact Marina Monticelli
Correspondent
Regulatory and Clinical Research Institute, Inc.
5353 Wayzata Blvd, Suite 505
Minneapolis,  MN  55416
Correspondent Contact Mary Beth Henderson
Regulation Number882.5330
Classification Product Code
GXN  
Subsequent Product Code
PJN  
Date Received02/27/2018
Decision Date 05/15/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-