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

Methyl Methacrylate For Aneurysmorrhaphy

21 CFR 882.5030 / Neurology
FDA source (opens on fda.gov)

JXH is the FDA product code for Methyl Methacrylate For Aneurysmorrhaphy, a class II device type, regulated under 21 CFR 882.5030. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JXH
Device name
Methyl Methacrylate For Aneurysmorrhaphy
Regulation
21 CFR 882.5030
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code JXH

By decision year
3 clearances under product code JXH with a decision year between 1987 and 2007, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JXH by decision year
YearClearances
19871
19881
20071

Applicants with the most clearances

Product code JXH
Applicants holding the most 510(k) clearances under product code JXH
ApplicantClearances
Cerenovus, Inc.1
Dentsply Intl.1
Karlin Technology, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code