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

Prosthesis, Intervertebral Disc

Unknown
FDA source (opens on fda.gov)

MJO is the FDA product code for Prosthesis, Intervertebral Disc, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 15 recalls.

Classification record

Product code
MJO
Device name
Prosthesis, Intervertebral Disc
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
15

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 66 companies shown, in name order