FDA 510(k) Applications Submitted by SURGICAL SPECIALTIES CORPORATION DBA ANGIOTECH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132268 | 07/22/2013 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN | SURGICAL SPECIALTIES CORPORATION DBA ANGIOTECH |
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