FDA 510(k), K071629, PARIETEX POLYESTER MESH WITH INTRODUCER

FDA 510(k), K071629, PARIETEX POLYESTER MESH WITH INTRODUCER

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510(K) Number: K071629
Device Name: PARIETEX POLYESTER MESH WITH INTRODUCER
Manufacturer: RENEE BORGESANO
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: KXA
Date Received: 06/14/2007
Decision Date: 07/10/2007
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

Total pages: 62  
Fully redacted pages: 8  
Content pages: 54 

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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.

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