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

Orthosis, Cervical-Thoracic, Rigid

21 CFR 890.3490 / Physical Medicine
FDA source (opens on fda.gov)

IQF is the FDA product code for Orthosis, Cervical-Thoracic, Rigid, a class I device type, regulated under 21 CFR 890.3490. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IQF
Device name
Orthosis, Cervical-Thoracic, Rigid
Regulation
21 CFR 890.3490
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
7
Ingested recalls
0

Clearances, product code IQF

By decision year
7 clearances under product code IQF with a decision year between 1978 and 1983, 1981 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code IQF by decision year
YearClearances
19782
19791
19813
19831

Applicants with the most clearances

Product code IQF
Applicants holding the most 510(k) clearances under product code IQF
ApplicantClearances
Orthomedics3
Hospital Products Co.1
Marullo, Baldwin, Frieden, Gatewood1
Medi-Ked, Inc.1
Zee Medical Products Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 77 companies shown, in name order