MODIFICATION AXIOM TOTAL KNEE SYST, PATELLAR COMP— 510(k) K912266

Name: FDA 510(k) clearance K912266
Creator: U.S. Food and Drug Administration
Published: 1991-08-20

Substantially Equivalent for Some Indications

Orothmet, Inc.

FDA 510(k) clearance K912266 for MODIFICATION AXIOM TOTAL KNEE SYST, PATELLAR COMP, Substantially Equivalent for Some Indications on 1991-08-20. Applicant: Orothmet, Inc.. Device class: 2.

Clearance details

Applicant: Orothmet, Inc.
Product code: Code JWH
Device class: Class 2
Regulation: 21 CFR 888.3560
Advisory panel: Orthopedic
Date received: 1991-05-22
Decision date: 1991-08-20
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JWH

view all

K262057 — GMK Extension2026-09-15
K260063 — GSPE Spacer2026-09-11
K262293 — EVOLUTION MPX Total Knee System2026-09-10
K262341 — b-ONE® Mobio Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem Extensions2026-09-08
K262130 — ATTUNE Revision Knee System2026-09-04

Adverse events under product code JWH

product code JWH

Death: 26
Injury: 51,564
Malfunction: 9,725
Other: 9
Total: 61,324

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.