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) (10)

Premarket Exempt

Clear

InterFuse S - 00819475010007 Catalog Number : 9076-06-20-0

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 - 00819475010014 Catalog Number : 9076-07-20-0

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 - 00819475010021 Catalog Number : 9076-08-20-0

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 - 00819475010038 Catalog Number : 9076-09-20-0

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 - 00819475010045 Catalog Number : 9076-10-20-0

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 - 00819475010052 Catalog Number : 9076-12-20-0

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 - 00819475010069 Catalog Number : 9076-14-20-0

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 - 00819475010076 Catalog Number : 9076-07-20-5

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 - 00819475010083 Catalog Number : 9076-08-20-5

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 - 00819475010090 Catalog Number : 9076-09-20-5

Device Description : Intervertebral Body Fusion Device

Device Class : 2

Duns Number: 362264421

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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