FDA 510K (K091299) SPECTRANETICS TURBO-TANDEM SYSTEM

FDA 510K (K091299) SPECTRANETICS TURBO-TANDEM SYSTEM

Regular price $241.73 USD
Regular price Sale price $241.73 USD
Sale Sold out

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

PLEASE NOTE: Most 510(k)s obtained through FOIA are heavily redacted, often omitting sections related to testing, software, manufacturing, and other technical data. Please be sure to review the total pages, redacted pages, and content pages listed in the description to get a sense of how much of the document is redacted. As the FDA FOIA office explains: “We HEAVILY REDACT the majority of the following portions of 510(k) filings: testing data, technical data, lab reports, manufacturing information, vendor information, substantive discussions regarding deficiencies or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.” If you’d like more details about a specific document before purchasing, please contact us at info@foiadocs.com.

View full details