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 T - 00819475010311 Catalog Number : 9091-12-20-0 -Q

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 - 00819475010328 Catalog Number : 9091-14-20-0 -Q

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 - 00819475010335 Catalog Number : 9091-11-20-0 -Q

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 - 00819475010342 Catalog Number : 9091-07-20-10-Q

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 - 00819475010359 Catalog Number : 9091-08-20-10-Q

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 - 00819475010366 Catalog Number : 9091-09-20-10-Q

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 - 00819475010373 Catalog Number : 9091-10-20-10-Q

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 - 00819475010380 Catalog Number : 9091-11-20-10-Q

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 - 00819475010397 Catalog Number : 9091-12-20-10-Q

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 - 00819475010403 Catalog Number : 9091-14-20-10-Q

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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