Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK VISTA INTERBODY FUSION CAGE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·DUAL INTERFIX-RP(TM) THREADED FUSION DEVICE

System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection

FDA classification

FDA Class 2 ·System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection

System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection

FDA classification

FDA Class 2 ·System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection

Shoulder Joint Humeral (Hemi-Shoulder) Ceramic Head/Metallic Stem Cemented Or Uncemented Prosthesis

FDA classification

FDA Class 2 ·Shoulder Joint Humeral (Hemi-Shoulder) Ceramic Head/Metallic Stem Cemented Or Uncemented Prosthesis

Filler, Bone Void, Alterable Compound For Cranioplasty

FDA classification

FDA Class 2 ·Filler, Bone Void, Alterable Compound For Cranioplasty

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·AUGMEN(TM) AKA SYNTHOGRAFT(TM) LG

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·SYNTHOGRAFT(TM) LARGE GRANULAR (LG)

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·SYNTHOGRAFT(TRICALCIUM PHOSPHATE-CERAMIC)

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·SYNTHOGRAFT(TRICALCIUM PHOSPHATE-CERAMIC)

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·SYNTHOGRAFT(TRICALCIUM PHOSPHATE-CERAMIC)

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·SYNTHOGRAFT(TRICALCIUM PHOSPHATE-CERAMIC)

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·PERI-OSS

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·SYNTHOGRAFT(TRICALCIUM PHOSPHATE-CERAMIC)

Implant, Endosseous, Root-Form

FDA Pre-Market Approval

FDA Class 2 ·ALVEOFORM TM BIOGRAFT

Surgical Film

FDA classification

FDA Class 2 ·Surgical Film

Filler, Bone Void, Non-Alterable Compound For Cranioplasty

FDA classification

FDA Class 2 ·Filler, Bone Void, Non-Alterable Compound For Cranioplasty

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection

FDA classification

FDA Class 2 ·System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection