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

Plinth

21 CFR 890.3520 / Physical Medicine
FDA source (opens on fda.gov)

INT is the FDA product code for Plinth, a class I device type, regulated under 21 CFR 890.3520. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
INT
Device name
Plinth
Regulation
21 CFR 890.3520
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
4
Ingested recalls
5

Clearances, product code INT

By decision year
4 clearances under product code INT with a decision year between 1977 and 1977, 1977 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code INT by decision year
YearClearances
19774

Applicants with the most clearances

Product code INT
Applicants holding the most 510(k) clearances under product code INT
ApplicantClearances
Will Ross Co.2
Chattanooga Pharmacal Co.1
I E Industries1

Companies listing this code with FDA

Companies whose registered establishments list this code