FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
26 MM CAST COCR HEAD AND POLYETHYLENE ACETABULAR SHELL LINER
K Number: K991622
·
Decision Jul 14, 1999
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
40
Review Days
64
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- 26 MM CAST COCR HEAD AND POLYETHYLENE ACETABULAR SHELL LINER
- K Number
- K991622
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3350
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Stelkast Company
- Date Received
- May 11, 1999
- Decision Date
- July 14, 1999
- Product Code
- JDI
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | FDA class 2 | Orthopedic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JDI), ordered by most recent decision date.
Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral Head
FDA 510(k)
FDA Class 2
·Orthopedic
Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners
FDA 510(k)
FDA Class 2
·Orthopedic
Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip Stems
FDA 510(k)
FDA Class 2
·Orthopedic
Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee Component
FDA 510(k)
FDA Class 2
·Orthopedic
Stryker Orthopaedics Hip Systems Labeling Update
FDA 510(k)
FDA Class 2
·Orthopedic
Global Modular Replacement System
FDA 510(k)
FDA Class 2
·Orthopedic
Other Clearances by Stelkast Company
| K Number | Device Name | ||
|---|---|---|---|
| K122883 | EXP TIBIAL INSERTS AND PATELLAR COMPONENTS FOR THE PROVEN GEN-FLEX TOTAL KNEE SYSTEM | Aug 5, 2013 | Substantially Equivalent |
| K122773 | CROSS-OVER ACETABULAR SHELL & LINER | Oct 9, 2012 | Substantially Equivalent |
| K094035 | EXP ACETABULAR LINER, MODELS SC3342 NON-HOODED 28MM, SC3343 HOODED 28MM | Mar 24, 2011 | Substantially Equivalent |
| K081458 | PROVEN STEM EXTENDER | Jun 6, 2008 | Substantially Equivalent |
| K063211 | PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT | Jan 18, 2007 | Substantially Equivalent |
| K051976 | PROVEN REVISION MODULAR TIBIAL TRAY | Oct 17, 2005 | Substantially Equivalent |
| K033944 | STELKAST 32MM MODULAR CERAMIC FEMORAL HEAD | Mar 12, 2004 | Substantially Equivalent |
| K032824 | STELKAST UNICONDYLAR KNEE SYSTEM | Nov 13, 2003 | Substantially Equivalent |
| K031901 | PROVEN REVISION FEMORAL AND PROVEN REVISION TIBIAL INSERT | Oct 10, 2003 | Substantially Equivalent |
| K032110 | PROCLASS PRESS FIT HIP STEM | Sep 22, 2003 | Substantially Equivalent |