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

Condylar Plate Fixation Implant

21 CFR 888.3030 / Orthopedic
FDA source (opens on fda.gov)

JDP is the FDA product code for Condylar Plate Fixation Implant, a class II device type, regulated under 21 CFR 888.3030. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
JDP
Device name
Condylar Plate Fixation Implant
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
2

Clearances, product code JDP

By decision year
2 clearances under product code JDP with a decision year between 2011 and 2017, 2011 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JDP by decision year
YearClearances
20111
20171

Applicants with the most clearances

Product code JDP
Applicants holding the most 510(k) clearances under product code JDP
ApplicantClearances
DePuy Synthes1
Synthes (USA) Products LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order