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

Support, Patient Position

21 CFR 868.6820 / Anesthesiology
FDA source (opens on fda.gov)

CCX is the FDA product code for Support, Patient Position, a class I device type, regulated under 21 CFR 868.6820. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and 7 recalls.

Classification record

Product code
CCX
Device name
Support, Patient Position
Regulation
21 CFR 868.6820
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
8
Ingested recalls
7

Clearances, product code CCX

By decision year
8 clearances under product code CCX with a decision year between 1980 and 1994, 1993 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code CCX by decision year
YearClearances
19801
19811
19821
19831
19861
19932
19941

Applicants with the most clearances

Product code CCX
Applicants holding the most 510(k) clearances under product code CCX
ApplicantClearances
American Medical Development, Inc.1
Body Therapeutics, Inc.1
Edward Carden1
Scientific Sales Intl., Inc.1
Sharn, Inc.1
Supportech, Inc.1
The Anspach Effort, Inc.1
Treace Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 266 companies shown, in name order