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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameCVX-300 EXCIMER LASER VERSION V3.7.12/V3.8.12
Classification Namedevice, removal, pacemaker electrode, percutaneous
ApplicantSPECTRANETICS CORP.
PMA NumberP960042
Supplement NumberS010
Date Received10/30/2008
Decision Date03/25/2009
Product Code
MFA[ Registered Establishments with MFA ]
Advisory Committee Cardiovascular
Supplement Type135 review track for 30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for: 1) removal of bioburden testing from the lot history records (lhr) as a test required for release of product, and 2) change lal endotoxin test procedure to instruct quality associates to collect product sample post-sterilization.
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