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U.S. Department of Health and Human Services

Devices@FDA
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceSYNVISC(HYLAN G-F 20)
Generic NameAcid, hyaluronic, intraarticular
ApplicantSanofi Genzyme Corp.
450 Water St.
Cambridge, MA 02141
PMA NumberP940015
Supplement NumberS007
Date Received03/29/2002
Decision Date04/26/2002
Product Code MOZ 
Advisory Committee Orthopedic
Supplement TypeSpecial (Immediate Track)
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR THE ADDITION OF THE FOLLOWING STATEMENT TO THE SYNVISC PHYSICIAN PACKAGE INSERT: "PRECAUTION: DO NOT OVER TIGHTEN OR APPLY EXCESSIVE LEVERAGE WHEN ATTACHING THE NEEDLE OR REMOVING THE NEEDLE GUARD, AS THIS MAY BREAK THE TIP OF THE SYRINGE."
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