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

Pusher, Socket

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

HXO is the FDA product code for Pusher, Socket, a class I device type, regulated under 21 CFR 888.4540. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
HXO
Device name
Pusher, Socket
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
3
Ingested recalls
1

Clearances, product code HXO

By decision year
3 clearances under product code HXO with a decision year between 1977 and 1989, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HXO by decision year
YearClearances
19771
19801
19891

Applicants with the most clearances

Product code HXO
Applicants holding the most 510(k) clearances under product code HXO
ApplicantClearances
Cobot Medical Corp.1
Depuy, Inc.1
Zimmer GmbH1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 68 companies shown, in name order