510(k) Report

FDA product code · Orthopedic

Prosthesis, Wrist, Carpal Lunate

KWNClass II21 CFR 888.3750510(k) required5 decisions since 19790 recalls

5 FDA decisions since 1979. No recall names this code. The most-cited predicate is K864491, named by 3 later devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, orthopedic panel

Twenty years of KWN at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · KWN

1in 2014

2008: 12014: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KWN

Too few KWN 510(k)s in any year since 2007 to give a median.

Recalls per year · KWN

No recall names KWN since 2007.

Adverse event reports per year · KWN

2in 2020

2007: 22010: 22013: 12016: 12017: 12018: 22019: 32020: 2
2007high 3 (2019) · low 0 (2008)2025

MAUDE reports naming product code KWN, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—02
20081—00
20090—00
20100—02
20110—00
20120—00
20130—01
20141—00
20150—00
20160—01
20170—01
20180—02
20190—03
20200—02
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — KWN by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in KWN? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report