BUECHEL-PAPPAS POLYETHLENE ACETABULAR COMPONENT(01-42-YYXX & 01-43-YYXX— 510(k) K960425
Substantially EquivalentEndotec, Inc.
FDA 510(k) clearance K960425 for BUECHEL-PAPPAS POLYETHLENE ACETABULAR COMPONENT(01-42-YYXX & 01-43-YYXX, Substantially Equivalent on 1996-10-03. Applicant: Endotec, Inc.. Device class: 2.
Clearance details
- Applicant
- Endotec, 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
- Bloomfield, NJ, US
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More clearances from Endotec, Inc.
view all- K081400 — FANNING-PAPPAS MODULAR KNEE BEARING
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- K992394 — BUECHEL-PAPPAS HUMERAL HEAD RESURFACING COMPONENT
- K982418 — BUECHEL-PAPPAS MODULAR SALVAGE STEM
- K963100 — TRONZO ACETABULAR FIXATION COMPONENT (1 99-02-00XX (ACE. FIXATION CUP) XX=OD OF ACE. CUP
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.