PEEK CAS

FDA 510(k)

FDA Class 2 ·Orthopedic

INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

MODIFICATION TO ALTIUS OCT SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

INTERPORE CROSS CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SYNERGY VLS CAP NUT MODELS 2206, 6102

FDA 510(k)

FDA Class 2 ·Orthopedic

TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODELS 8123, 8124, 8132, 8133, 8156, 8157, 8158, & 8189

FDA 510(k)

FDA Class 2 ·Orthopedic

ACCESS CONCENTRATION SYSTEM, MODEL ACC-100, ACCESS DISPOSABLE SET, MODEL ADS-2000

FDA 510(k)

FDA Class 2 ·Anesthesiology

APPLICATOR TIP/DUAL SPRAYER KIT

FDA 510(k)

FDA Class 2 ·General Hospital

PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,

FDA 510(k)

FDA Class 2 ·Orthopedic

GEO STRUCTURE

FDA 510(k)

FDA Class 2 ·Orthopedic

PRO OSTEON 200R WITH CALCIUM SULFATE, MODELS 2RCS038, 2RCS050, 2RCS075, 2RCS10, 2RCS15, 2RCS20, 2RCS225, 2RCS30

FDA 510(k)

FDA Class 2 ·Orthopedic

SYNERGY TI INTEGRAL OPEN SCREWS MODELS # 6193, 6194, 6195,6196, 6173, 6174, 6175, 6176, 6177

FDA 510(k)

FDA Class 2 ·Orthopedic

MODIFICATION TO GEO STRUCTURE

FDA 510(k)

FDA Class 2 ·Orthopedic

SYNERGY D2 SPINAL IMPLANTS

FDA 510(k)

FDA Class 2 ·Orthopedic

PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE

FDA 510(k)

FDA Class 2 ·Orthopedic

SYNERGY INTEGRAL SCREWS, MODELS, 2161,2162,2163,2164,2165,2166,2167,2168,2169,2210,2211,2212,2215,2216,2217,2220,2221,22

FDA 510(k)

FDA Class 2 ·Orthopedic

INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)

FDA 510(k)

FDA Class 2 ·Orthopedic

SYNERGY 4.0 MM, 4.5 MM VLS SCREWS

FDA 510(k)

FDA Class 2 ·Orthopedic

MODIFICATION TO TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODEL 8130, 8131

FDA 510(k)

FDA Class 2 ·Orthopedic

OSTEOPLAST, MODEL POP200

FDA 510(k)

FDA Class 2 ·Orthopedic