510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K913765Substantially Equivalent

Yasargil Aneurysm Clips, Modification

Aesculap Inc, South San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913765 is the FDA 510(k) clearance record for YASARGIL ANEURYSM CLIPS, MODIFICATION, a class II device, cleared for Aesculap, Inc. on under FDA product code HCH (Clip, Aneurysm). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K913765.

Clearance record

Decision date
Received
(202 days to decision)
Product code
HCH Clip, Aneurysm
Regulation
21 CFR 882.5200
Device class
Class II
Review panel
Neurology
Applicant
Aesculap, Inc. 1000 Gateway Blvd., South San Francisco CA
510(k) summary
Statement
Third party review
No

Clearances, product code HCH

Trailing 12 months

FDA records hold no clearances under product code HCH in the trailing twelve months.

FDA records show no clearances under product code HCH in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HCH, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260