VERTEBRAL TECHNOLOGIES, INC.

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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) (8)

Premarket Exempt

Clear

InterFuse L - 00819475010915 Catalog Number : 9119-14-21-50-8

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse L - 00819475010922 Catalog Number : 9119-14-21-55-8

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse S - 00819475010939 Catalog Number : 9076-13-20-0

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse S - 00819475010946 Catalog Number : 9076-13-20-5

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse S - 00819475010953 Catalog Number : 9076-13-20-0-B

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse S - 00819475010960 Catalog Number : 9076-13-20-5-B

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse T - 00819475010977 Catalog Number : 9091-13-20-0

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

InterFuse T - 00819475010984 Catalog Number : 9091-13-20-10

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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