2,866 results · 39ms · Sources: EU EUDAMED, US FDA

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

Bone Cement

FDA Pre-Market Approval
FDA Class 2 ·PALACOS R BONE CEMENT

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE

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

FDA Pre-Market Approval
FDA Class 2 ·WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS

Bone Cement

FDA Pre-Market Approval
FDA Class 2 ·PALACOS E-FLOW (OSTEOPAL) BONE CEMENT

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX TM THREADED FUSION DEVICE

Accessories, Soft Lens Products

FDA Pre-Market Approval
FDA Class 2 ·EASY EYES (TM)

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·LT-CAGE LUMBAR TAPERED FUSION DEVICE (TI AND PEEK)

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·SOFTACT(TM) (DELTAFILCON A)

Bone Cement

FDA Pre-Market Approval
FDA Class 2 ·PALACOS R BONE CEMENT

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX THREADED FUSION DEVICE

Accessories, Soft Lens Products

FDA Pre-Market Approval
FDA Class 2 ·EASY EYES (TM)

Bone Cement

FDA Pre-Market Approval
FDA Class 2 ·PALACOS R BONE CEMENT

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·SOFTACT II (POLYMACON)

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX THREADED FUSION DEVICE

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·SOFTACT II (POLYMACON)

Accessories, Soft Lens Products

FDA Pre-Market Approval
FDA Class 2 ·EASY EYES (TM)

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·SOFTACT II (POLYMACON)

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·LT-CAGE LUMBAR TAPERED FUSION DEVICE