FDA 510K (K091299) SPECTRANETICS TURBO-TANDEM SYSTEM
FDA 510K (K091299) SPECTRANETICS TURBO-TANDEM SYSTEM
Device Classification Name Catheter, Percutaneous
510(k) Number K091299
Device Name SPECTRANETICS TURBO-TANDEM SYSTEM
Applicant SPECTRANETICS CORP.
Regulation Number 870.1250
Classification Product Code DQY
Date Received 05/04/2009
Decision Date 07/01/2009
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
Total pages: 588
Fully redacted pages: 509
Content pages: 79
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