S-ROM TOTAL HIP REPLACEMENT SYSTEM— 510(k) K920739

Substantially Equivalent for Some Indications

Joint Medical Products Corp.

FDA 510(k) clearance K920739 for S-ROM TOTAL HIP REPLACEMENT SYSTEM, Substantially Equivalent for Some Indications on 1992-11-24. Applicant: Joint Medical Products Corp..

Clearance details

Applicant
Joint Medical Products Corp.
Product code
Code JDI
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent for Some Indications
Clearance type
Traditional
Location
Stamford, CT, US
Download summary PDFView on FDA.gov ↗

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.