PROFEMUR XTR HIP STEM— 510(k) K052915

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K052915 for PROFEMUR XTR HIP STEM, Substantially Equivalent on 2006-01-27. Applicant: Wrightmedicaltechnologyinc. Device class: 3.

Clearance details

Applicant
Wrightmedicaltechnologyinc
Product code
Code KWA
Device class
Class 3
Regulation
21 CFR 888.3330
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Arlington, TN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code KWA

product code KWA
Death
38
Injury
10,439
Malfunction
1,862
Total
12,339

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 K052915

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 K052915.

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