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

Premarket Approval (PMA)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | 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.
 
Trade NameGEL-ONE
Classification Nameacid, hyaluronic, intraarticular
ApplicantSEIKAGAKU CORP.
PMA NumberP080020
Date Received07/31/2008
Decision Date03/22/2011
Product Code
MOZ[ Registered Establishments with MOZ ]
Docket Number 11M-0198
Notice Date 03/31/2011
Advisory Committee Orthopedic
Clinical Trials NCT00449696
NCT00450112
Expedited Review Granted? No
Combination Product No
Information About: Labeling, Approval Order, Summary of Safety and Effectiveness
Approval Order Statement 
Approval for the gel-one. The device is indicated for the treatment of pain in osteoarthritis (oa) of the knee in patients who have failed to respond adequately to non-pharmacologic therapy, non-steroidal anti-inflammatory drugs (nsaids) or analgesics, e. G. , acetaminophen.
Approval Order Approval Order
Supplements: S001 S002 S003 S004 
-
-