510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873688Substantially Equivalent

Aneuroplastic, Acrylic Aneuryomorrhaply Material

Dentsply Intl., York PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873688 is the FDA 510(k) clearance record for ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL, a class II device, cleared for Dentsply Intl. on under FDA product code JXH (Methyl Methacrylate For Aneurysmorrhaphy). FDA records list 291 510(k) clearances for Dentsply Intl., from to . As of , FDA records show no recalls naming K873688.

Clearance record

Decision date
Received
(46 days to decision)
Product code
JXH Methyl Methacrylate For Aneurysmorrhaphy
Regulation
21 CFR 882.5030
Device class
Class II
Review panel
Neurology
Applicant
Dentsply Intl. 570 W. College Ave., York PA
Third party review
No

Clearances, product code JXH

Trailing 12 months

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

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