510(k) Report

FDA product code · Ear, nose and throat

Ear, Nose, And Throat Stereotaxic Instrument

PGWClass II21 CFR 882.4560510(k) required38 decisions since 20146 recalls

38 FDA decisions since 2014. 510(k) reviews decided 2021–2025 took a median of 97 days (half between 84 and 127). 6 recalls name this code, 0 of them Class I. The most-cited predicate is K133573, named by 8 later devices.

Intended as an aid for precisely locating a surgical instrument within anatomical structures in either open or percutaneous procedures for any medical condition in which a reference to a rigid anatomical structure in the field of ENT surgery can be identified relative to a CT- or MR-based model or digitized landmarks of the anatomy.

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, ear, nose and throat panel

Twenty years of PGW 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 · PGW

1in 2025

2014: 42015: 12016: 92017: 42018: 22019: 12020: 82021: 12022: 22023: 22025: 12026 (partial year): 3
2007high 9 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PGW

100in 2020

2014: 116 days median2016: 115 days median2017: 125 days median2020: 100 days median2026 (partial year): 65 days median
2007high 125 (2017) · low 100 (2020)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · PGW

1in 2025

2019: 32021: 12023: 12025: 1
2007high 3 (2019) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · PGW

220in 2025

2014: 72015: 142016: 332017: 422018: 962019: 2472020: 1612021: 1902022: 1662023: 2002024: 2742025: 220
2007high 274 (2024) · low 0 (2007)2025

MAUDE reports naming product code PGW, 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—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
2014411607
20151—014
20169115033
20174125042
20182—096
20191—3247
202081000161
20211—1190
20222—0166
20232—1200
20240—0274
20251—1220
20263650—
FIG. 1 — PGW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in PGW? 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

Related product codes

Other codes under 21 CFR 882.4560.