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 - 00818956021105 Catalog Number : 100001-637

Device Description : Spinal Jaxx Implant, 11Hx10Wx35L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021112 Catalog Number : 100001-638

Device Description : Spinal Jaxx Implant, 11Hx12Wx35L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021129 Catalog Number : 100001-639

Device Description : Spinal Jaxx Implant, 13Hx10Wx23L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021136 Catalog Number : 100001-640

Device Description : Spinal Jaxx Implant, 13Hx12Wx23L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021143 Catalog Number : 100001-641

Device Description : Spinal Jaxx Implant, 13Hx10Wx27L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021150 Catalog Number : 100001-642

Device Description : Spinal Jaxx Implant, 13Hx12Wx27L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021167 Catalog Number : 100001-643

Device Description : Spinal Jaxx Implant, 13Hx10Wx31L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021174 Catalog Number : 100001-644

Device Description : Spinal Jaxx Implant, 13Hx12Wx31L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021181 Catalog Number : 100001-645

Device Description : Spinal Jaxx Implant, 13Hx10Wx35L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956021198 Catalog Number : 100001-646

Device Description : Spinal Jaxx Implant, 13Hx12Wx35L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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