NEUROPRO SPINAL JAXX INC.

Address:6337 Falling Brook Dr,Burke,VA,22015,US

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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

Spinal Jaxx Interbody Fusion Device - 00818956021006 Catalog Number : 100001-627

Device Description : Spinal Jaxx Implant, 9Hx10Wx31L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021013 Catalog Number : 100001-628

Device Description : Spinal Jaxx Implant, 9Hx12Wx31L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021020 Catalog Number : 100001-629

Device Description : Spinal Jaxx Implant, 9Hx10Wx35L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021037 Catalog Number : 100001-630

Device Description : Spinal Jaxx Implant, 9Hx12Wx35L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021044 Catalog Number : 100001-631

Device Description : Spinal Jaxx Implant, 11Hx10Wx23L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021051 Catalog Number : 100001-632

Device Description : Spinal Jaxx Implant, 11Hx12Wx23L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021068 Catalog Number : 100001-633

Device Description : Spinal Jaxx Implant, 11Hx10Wx27L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021075 Catalog Number : 100001-634

Device Description : Spinal Jaxx Implant, 11Hx12Wx27L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021082 Catalog Number : 100001-635

Device Description : Spinal Jaxx Implant, 11Hx10Wx31L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021099 Catalog Number : 100001-636

Device Description : Spinal Jaxx Implant, 11Hx12Wx31L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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