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

Hook, Bone

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

KIK is the FDA product code for Hook, Bone, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KIK
Device name
Hook, Bone
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
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 KIK

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

Applicants with the most clearances

Product code KIK
Applicants holding the most 510(k) clearances under product code KIK
ApplicantClearances
Depuy, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 107 companies shown, in name order