SEARCH RESULTS FOR: seaspine(90 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (90)

Brand Name

• Regatta Lateral System (90)

GMDN Term Name

• Vertebral body prosthesis (90)

GMDN Term Status

• Active (90)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (90)

FDA Product Code

• MAX (90)

Device Packaged As Sterile

• Yes (90)

Sterilization Prior To Use

• No (90)

Issuing Agency

• GS1 (90)

Device Size Type

• 18mm x 10mm x 40mm, 0 Deg (1)
• 18mm x 10mm x 40mm, 10 Deg (1)
• 18mm x 10mm x 45mm, 0 Deg (1)
• 18mm x 10mm x 45mm, 10 Deg (1)
• 18mm x 10mm x 45mm, 15 Deg (1)
• 18mm x 10mm x 50mm, 0 Deg (1)
• 18mm x 10mm x 50mm, 10 Deg (1)
• 18mm x 10mm x 50mm, 15 Deg (1)
• 18mm x 10mm x 55mm, 10 Deg (1)
• 18mm x 10mm x 55mm, 15 Deg (1)
• 18mm x 10mm x 60mm, 10 Deg (1)
• 18mm x 10mm x 60mm, 15 Deg (1)
• 18mm x 12mm x 40mm, 0 Deg (1)
• 18mm x 12mm x 40mm, 10 Deg (1)
• 18mm x 12mm x 45mm, 0 Deg (1)
• 18mm x 12mm x 45mm, 10 Deg (1)
• 18mm x 12mm x 45mm, 15 Deg (1)
• 18mm x 12mm x 50mm, 0 Deg (1)
• 18mm x 12mm x 50mm, 10 Deg (1)
• 18mm x 12mm x 50mm, 15 Deg (1)
• 18mm x 12mm x 55mm, 10 Deg (1)
• 18mm x 12mm x 55mm, 15 Deg (1)
• 18mm x 12mm x 60mm, 10 Deg (1)
• 18mm x 12mm x 60mm, 15 Deg (1)
• 18mm x 14mm x 40mm, 0 Deg (1)
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Device Class

• Class II (90)

Implantable

• Yes (90)