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

Wax, Bone

Unknown
FDA source (opens on fda.gov)

MTJ is the FDA product code for Wax, Bone. As of , FDA records hold 42 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
MTJ
Device name
Wax, Bone
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
43
Ingested recalls
4

Clearances, product code MTJ

By decision year
43 clearances under product code MTJ with a decision year between 1979 and 2026, 2011 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code MTJ by decision year
YearClearances
19791
19971
20001
20031
20041
20054
20062
20081
20092
20101
20115
20123
20132
20144
20152
20162
20191
20201
20211
20221
20234
20262

Applicants with the most clearances

Product code MTJ
Applicants holding the most 510(k) clearances under product code MTJ
ApplicantClearances
Orthocon, Inc.23
Ceremed, Inc.6
Cp Medical2
Aesculap Inc1
Hemostasis, LLC1
Lukens Corp.1
M/s. Meril Endo Surgery Private Limited.1
Marine Polymer Technologies, Inc.1
Orthocon, Inc.1
Resorbable Orthopedic Products, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 25 companies shown, in name order