510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K202124Substantially Equivalent

Aesculap PAS-Port Proximal Anastomosis System

Aesculap Inc, Center Valley PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K202124 is the FDA 510(k) clearance record for Aesculap PAS-Port Proximal Anastomosis System, a class II device, cleared for Aesculap, Inc. on under FDA product code FZP (Clip, Implantable). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show 2 recalls naming K202124.

Clearance record

Decision date
Received
(33 days to decision)
Product code
FZP Clip, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Aesculap, Inc. 3773 Corporate Pkwy., Center Valley PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FZP

Trailing 12 months
5 clearances under product code FZP in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FZP, trailing twelve months
MonthClearances
November 20251
December 20252
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20261
October 20260