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

Component, Traction, Non-Invasive

21 CFR 888.5890 / Orthopedic
FDA source (opens on fda.gov)

KQZ is the FDA product code for Component, Traction, Non-Invasive, a class I device type, regulated under 21 CFR 888.5890. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and 9 recalls.

Classification record

Product code
KQZ
Device name
Component, Traction, Non-Invasive
Regulation
21 CFR 888.5890
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
11
Ingested recalls
9

Clearances, product code KQZ

By decision year
11 clearances under product code KQZ with a decision year between 1978 and 1988, 1982 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KQZ by decision year
YearClearances
19781
19801
19823
19831
19851
19872
19882

Applicants with the most clearances

Product code KQZ
Applicants holding the most 510(k) clearances under product code KQZ
ApplicantClearances
Warm & Form, Orthopedic Materials2
Avec Scientific Design Corp.1
Backtrac1
Comfortex, Inc.1
Depuy, Inc.1
Howmedica Corp.1
Physical Diagnostics, Inc.1
Technol, Inc.1
Tecnol New Jersey Wound Care, Inc.1
The Kendal Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 105 companies shown, in name order