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

Catheter, Percutaneous, Intraspinal, Short Term

21 CFR 868.5120 / Anesthesiology
FDA source (opens on fda.gov)

MAJ is the FDA product code for Catheter, Percutaneous, Intraspinal, Short Term, a class II device type, regulated under 21 CFR 868.5120. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MAJ
Device name
Catheter, Percutaneous, Intraspinal, Short Term
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
6
Ingested recalls
0

Clearances, product code MAJ

By decision year
6 clearances under product code MAJ with a decision year between 1989 and 1997, 1995 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MAJ by decision year
YearClearances
19891
19911
19931
19952
19971

Applicants with the most clearances

Product code MAJ
Applicants holding the most 510(k) clearances under product code MAJ
ApplicantClearances
Medtronic, Inc.3
Abbott Medical1
Concord/Portex1
Pudenz-Schulte Medical Research Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code