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

Positioner, Socket

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

KIL is the FDA product code for Positioner, Socket, 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 no recalls.

Classification record

Product code
KIL
Device name
Positioner, 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
1
Ingested recalls
0

Clearances, product code KIL

By decision year
1 clearance under product code KIL with a decision year between 1993 and 1993, 1993 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KIL by decision year
YearClearances
19931

Applicants with the most clearances

Product code KIL
Applicants holding the most 510(k) clearances under product code KIL
ApplicantClearances
voss medical products1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 35 companies shown, in name order