Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
FDA product code OQG · 16 cleared devices
- Regulation
- 21 CFR 888.3358
- Review panel
- OR
- Implant
- Yes
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2011-03-24 – 2021-08-20
1. Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis. 3. Correction of functional deformity. 4. Treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable by other techniques. 5. Revision procedures where other treatment or devices have failed. Cemented and uncemented use.
KMTI Hip Replacement System
View details →KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System
View details →Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System
View details →FMP Extended Liners
View details →Renovis Surgical Hip Replacement System
View details →Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile Acetabular Insert with E-Link® Poly
View details →VITALITE E CROSS-LINKED POLYETHYLENE ACETABULAR INSERT
View details →PLASMAFIT ACETABULAR CUP AND VITELENE INSERT
View details →X-ALT HIGHLY CROSS LINKED VE ACETABULAR LINER
View details →PBP TOTAL HIP SYSTEM
View details →CROSS-OVER ACETABULAR SHELL & LINER
View details →RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS
View details →VIVACIT-E VITAMIN E HIGHLY CROSSLINKED POLYETHYLENE LINERS
View details →PIPELINE TOTAL HIP SYSTEM
View details →EXP ACETABULAR LINER, MODELS SC3342 NON-HOODED 28MM, SC3343 HOODED 28MM
View details →No matching devices.
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