Biomet Proximal Humerus Plating System— 510(k) K143697

Substantially Equivalent

Biomet Manufacturing

FDA 510(k) clearance K143697 for Biomet Proximal Humerus Plating System, Substantially Equivalent on 2015-03-30. Applicant: Biomet Manufacturing. Device class: 2.

Clearance details

Applicant
Biomet Manufacturing
Product code
Code HRS
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Warsaw, IN, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code HRS

view all

Adverse events under product code HRS

product code HRS
Death
27
Injury
10,340
Malfunction
3,328
Total
13,695

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

Recalls naming K143697

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K143697.

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