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

Tamp

21 CFR 888.4540 / Orthopedic
FDA source (opens on fda.gov)

HXG is the FDA product code for Tamp, a class I device type, regulated under 21 CFR 888.4540. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
HXG
Device name
Tamp
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code HXG

By decision year
1 clearance under product code HXG with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HXG by decision year
YearClearances
19841

Applicants with the most clearances

Product code HXG
Applicants holding the most 510(k) clearances under product code HXG
ApplicantClearances
Plastafil, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 213 companies shown, in name order