OPTIMESH 500E CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

OMNIFLEX-C UHMWPE MID-SHAFT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Biocore9 Femoral Head Resurfacing Component

FDA 510(k)

FDA Class 2 ·Orthopedic

TITANIUM CEMENT RESTRICTOR MATERIAL PEEK

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

PROXIMAL CEMENT SPACER

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

BONE CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

RECAP HA PRESS-FIT FEMORAL RESURFACING HEAD

FDA 510(k)

FDA Class 2 ·Orthopedic

METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

CEMENTED FEMORAL HEAD RESURFING DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

SPINAL USA CEMENT RESTRICTOR SYSTEM

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SKELITE RESORBABLE CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

MODUILAR UNIPOLAR

FDA 510(k)

FDA Class 2 ·Orthopedic

FIDJI SMALL CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval

FDA Class 2 ·GENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval

FDA Class 2 ·GENESIS HOME UTERINE ACTIVITY MONITORING SYSTEM (HUAM)

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval

FDA Class 2 ·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval

FDA Class 2 ·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

FDA Pre-Market Approval

FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED LINER

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

FDA Pre-Market Approval

FDA Class 2 ·DURALOC(TM) 300S ACETABULAR CUP WITH POROCOAT(TM)

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

FDA Pre-Market Approval

FDA Class 2 ·AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS