MODIFIED LSF TOTAL HIP SYSTEM— 510(k) K884432

Substantially Equivalent

Implant Technology, Inc.

FDA 510(k) clearance K884432 for MODIFIED LSF TOTAL HIP SYSTEM, Substantially Equivalent on 1988-12-09. Applicant: Implant Technology, Inc.. Device class: 2.

Clearance details

Applicant
Implant Technology, Inc.
Product code
Code JDI
Device class
Class 2
Regulation
21 CFR 888.3350
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Secaucus, NJ, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code JDI

product code JDI
Death
65
Injury
12,943
Malfunction
1,681
Total
14,689

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 →

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