SL-PLUS AND SLR-PLUS STEMS— 510(k) K001942
Substantially EquivalentPlus Orthopedics
FDA 510(k) clearance K001942 for SL-PLUS AND SLR-PLUS STEMS, Substantially Equivalent on 2000-07-25. Applicant: Plus Orthopedics.
Clearance details
- Applicant
- Plus Orthopedics
- Product code
- Code LWJ
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- San Diego, CA, US
Adverse events under product code LWJ
product code LWJ- Injury
- 544
- Total
- 544
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.