The following data is part of a premarket notification filed by Angiotech with the FDA for Quill Pdo Knotless Tissue-closure Device (polydixanone).
Device ID | K120827 |
510k Number | K120827 |
Device Name: | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE) |
Classification | Suture, Surgical, Absorbable, Polydioxanone |
Applicant | ANGIOTECH 100 DENNIS DRIVE Reading, PA 19606 |
Contact | Kirsten Stowell |
Correspondent | Kirsten Stowell ANGIOTECH 100 DENNIS DRIVE Reading, PA 19606 |
Product Code | NEW |
CFR Regulation Number | 878.4840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-03-19 |
Decision Date | 2012-07-13 |
Summary: | summary |