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

Prosthesis, Shoulder, Humeral (Bipolar Hemi-Shoulder) Metal/Polymer, Cemented Or Uncemented

Unknown
FDA source (opens on fda.gov)

MJT is the FDA product code for Prosthesis, Shoulder, Humeral (Bipolar Hemi-Shoulder) Metal/Polymer, Cemented Or Uncemented, a class III device type. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MJT
Device name
Prosthesis, Shoulder, Humeral (Bipolar Hemi-Shoulder) Metal/Polymer, Cemented Or Uncemented
Device class
Class III
Review panel
Unknown
Submission type
Contact ODE
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code MJT

By decision year
3 clearances under product code MJT with a decision year between 1997 and 1999, 1999 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MJT by decision year
YearClearances
19971
19992

Applicants with the most clearances

Product code MJT
Applicants holding the most 510(k) clearances under product code MJT
ApplicantClearances
Zimmer GmbH1
Endotec, Inc.1
Howmedica Osteonics Corp1

Companies listing this code with FDA

Companies whose registered establishments list this code