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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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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.
 
DeviceCOAPTITE INJECTABLE IMPLANT
Generic NameAGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
ApplicantMerz North America, Inc.
4133 Ct.ney Rd., Suite 10
Franksville, WI 53126
PMA NumberP040047
Supplement NumberS021
Date Received07/25/2011
Decision Date05/17/2012
Product Code LNM 
Advisory Committee Gastroenterology/Urology
Supplement Type135 Review Track For 30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL TO REPLACE THE PIN GAUGE TEST WITH A PLUNGER CONTACT TEST AND TO REPLACE THE MANUAL WAY OF MEASURING THE LUER END OF THE SYRINGE BARREL WITH A CALIBRATED LUER GAUGE.
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