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

Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained

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FDA source (opens on fda.gov)

LZJ is the FDA product code for Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LZJ
Device name
Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained
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
11
Ingested recalls
1

Clearances, product code LZJ

By decision year
11 clearances under product code LZJ with a decision year between 1989 and 2014, 1993 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LZJ by decision year
YearClearances
19891
19911
19921
19932
19942
19951
20081
20101
20141

Applicants with the most clearances

Product code LZJ
Applicants holding the most 510(k) clearances under product code LZJ
ApplicantClearances
Acu Med, Inc.2
Zimmer GmbH2
Arthrosurface, Inc.1
Ascension Orthopedics, Inc.1
Dow Corning Wright1
Kinetikos Medical, Inc.1
Merete GmbH1
Orthopaedic Biosystems, Ltd.1
Osteomed1

Companies listing this code with FDA

Companies whose registered establishments list this code