• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • 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
Note: this medical device has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
DeviceTMJ FOSSA-EMINENCE PROSTHESIS(TM)
Classification Nameglenoid fossa prosthesis
Generic Nameglenoid fossa prosthesis
Regulation Number872.3950
Applicant
NEXUS CMF, LLC
17301 west colfax avenue
suite 170
golden, CO 80401
PMA NumberP000035
Date Received06/20/2000
Decision Date02/27/2001
Product Code
MPI[ Registered Establishments with MPI ]
Docket Number 01M-0210
Notice Date 05/14/2001
Advisory Committee Dental
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the tmj fossa-eminence prosthesis(tm). The device is indicated for use in treatment of severe temporomandibular joint disease due to: 1) inflammatory arthritis involving the temporomandibular joint not responsive to other modalities of treatment, 2) recurrent fibrosis and/or bony ankylosis not responsive to other modalities of treatment, 3) failed tissue graft, 4) failed alloplastic joint reconstruction, 5) internal derangement confirmed to be pathological in origin by both clinical observation and radiographic findings, where the patient has moderate to severe pain and/or disabling dysfunction and has not responded to less invasive conventional therapy.
Approval Order Approval Order
Summary Summary of Safety and Effectiveness
Labeling Labeling
Labeling Part 2
Post-Approval StudyShow Report Schedule and Study Progress
Supplements: S001 S002 S003 S004 S006 S007 S008 S009 S010 
S011 
-
-