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

Implant, Temporal

21 CFR 878.3550 / General, Plastic Surgery
FDA source (opens on fda.gov)

MNF is the FDA product code for Implant, Temporal, a class II device type, regulated under 21 CFR 878.3550. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MNF
Device name
Implant, Temporal
Regulation
21 CFR 878.3550
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code MNF

By decision year
2 clearances under product code MNF with a decision year between 2000 and 2011, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MNF by decision year
YearClearances
20001
20111

Applicants with the most clearances

Product code MNF
Applicants holding the most 510(k) clearances under product code MNF
ApplicantClearances
Osteosymbionics, LLC1
Porex Surgical Products Group1

Companies listing this code with FDA

Companies whose registered establishments list this code