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

Prosthesis, Wrist, Carpal Scaphoid

21 CFR 888.3760 / Orthopedic
FDA source (opens on fda.gov)

KWO is the FDA product code for Prosthesis, Wrist, Carpal Scaphoid, a class II device type, regulated under 21 CFR 888.3760. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KWO
Device name
Prosthesis, Wrist, Carpal Scaphoid
Regulation
21 CFR 888.3760
Device class
Class II
Review panel
Orthopedic
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code KWO

By decision year
1 clearance under product code KWO with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KWO by decision year
YearClearances
19871

Applicants with the most clearances

Product code KWO
Applicants holding the most 510(k) clearances under product code KWO
ApplicantClearances
Dow Corning Wright1

Companies listing this code with FDA

Companies whose registered establishments list this code