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

Cutter, Wire

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

HXZ is the FDA product code for Cutter, Wire, 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 one recall.

Classification record

Product code
HXZ
Device name
Cutter, Wire
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
1

Clearances, product code HXZ

By decision year
1 clearance under product code HXZ with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HXZ by decision year
YearClearances
19871

Applicants with the most clearances

Product code HXZ
Applicants holding the most 510(k) clearances under product code HXZ
ApplicantClearances
Military Engineering, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 236 companies shown, in name order