• 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 Appliance, Fixation, Spinal Interlaminal
510(k) Number K931225
Device Name LOW PROFILE MID CROSS BRACING
Applicant
Advanced Spine Fixation Systems, Inc.
11095 Knott Ave.
Suite L
Cypress,  CA  90630
Applicant Contact ROBERT S HOWLAND
Correspondent
Advanced Spine Fixation Systems, Inc.
11095 Knott Ave.
Suite L
Cypress,  CA  90630
Correspondent Contact ROBERT S HOWLAND
Regulation Number888.3050
Classification Product Code
KWP  
Date Received03/10/1993
Decision Date 05/02/1994
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-