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

Needle, Spinal, Short Term

21 CFR 868.5150 / Anesthesiology
FDA source (opens on fda.gov)

MIA is the FDA product code for Needle, Spinal, Short Term, a class II device type, regulated under 21 CFR 868.5150. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MIA
Device name
Needle, Spinal, Short Term
Regulation
21 CFR 868.5150
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
10
Ingested recalls
0

Clearances, product code MIA

By decision year
10 clearances under product code MIA with a decision year between 1993 and 2018, 1996 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MIA by decision year
YearClearances
19931
19941
19962
19972
19981
19991
20051
20181

Applicants with the most clearances

Product code MIA
Applicants holding the most 510(k) clearances under product code MIA
ApplicantClearances
Abbott Medical2
Acufex Microsurgical, Inc.1
Medtronic, Inc.1
Avid N.I.T., Inc.1
Custom Medical Concepts, Inc.1
Epimed International, Inc.1
Global Medical Prods, Inc.1
Klein-Baker Medical, Inc.1
Promex, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 18 companies shown, in name order