510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K132268Substantially Equivalent

Quill Pdo Knotless Tissue-Closure Device, Variable Loop Design

Surgical Specialties Corporation dba Angiotech, Reading PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132268 is the FDA 510(k) clearance record for QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN, a class II device, cleared for Surgical Specialties Corporation Dba Angiotech on under FDA product code NEW (Suture, Surgical, Absorbable, Polydioxanone). FDA records list one 510(k) clearance for Surgical Specialties Corporation Dba Angiotech. As of , FDA records show no recalls naming K132268.

Clearance record

Decision date
Received
(32 days to decision)
Product code
NEW Suture, Surgical, Absorbable, Polydioxanone
Regulation
21 CFR 878.4840
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Surgical Specialties Corporation Dba Angiotech 100 Dennis Dr., Reading PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NEW

Trailing 12 months
6 clearances under product code NEW in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NEW, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20261
August 20261
September 20261
October 20260