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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.
 
DeviceHEMOBLAST™ Bellows
Generic NameAbsorbable collagen hemostatic agent with thrombin
Regulation Number878.4490
ApplicantDilon Technologies, Inc.
12050 Jefferson Ave., Suite 340
Newport News, VA 23606
PMA NumberP170012
Supplement NumberS012
Date Received10/30/2018
Decision Date11/29/2018
Product Code PMX 
Advisory Committee General & Plastic Surgery
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductYes
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
1. Change of agitation schedule for first delipidation/dehydration acetone soak in the production of The Basic Fibrous Collagen; and2. Addition of a stirrer to be employed in the Pre-Grinding Baths in the production of The Basic Fibrous Collagen.
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