SPINEOLOGY INC.

Address:7800 THIRD STREET N.,Saint Paul,MN,55128,US

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Filters

Device Class

Class-1 (A medical device with low to moderate risk that requires general controls) Class-2 (A medical device with a moderate to high risk that requires special controls) Class-3 (A medical device with high risk that requires premarket approval) Class-U (Unclassified)

Product Code

Intervertebral fusion device with bone graft, lumbar (MAX) (5)

Premarket Exempt

Clear

Rampart-O - M9403802512 Catalog Number : 380-2512

Device Description : Asm, Rampart-O

Device Class : 2

Duns Number: 033014361

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Rampart-O - M9403802513 Catalog Number : 380-2513

Device Description : Asm, Rampart-O

Device Class : 2

Duns Number: 033014361

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Rampart-O - M9403802514 Catalog Number : 380-2514

Device Description : Asm, Rampart-O

Device Class : 2

Duns Number: 033014361

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Rampart-O - M9403802515 Catalog Number : 380-2515

Device Description : Asm, Rampart-O

Device Class : 2

Duns Number: 033014361

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Rampart-O - M9403802516 Catalog Number : 380-2516

Device Description : Asm, Rampart-O

Device Class : 2

Duns Number: 033014361

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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