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) (4)

Premarket Exempt

Clear

Spinal Jaxx Interbody Fusion Device - 00818956021402 Catalog Number : 100001-578

Device Description : Spinal Jaxx OsteoSync 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 - 00818956021419 Catalog Number : 100001-579

Device Description : Spinal Jaxx OsteoSync 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 - 00818956021426 Catalog Number : 100001-580

Device Description : Spinal Jaxx OsteoSync 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 - 00818956021433 Catalog Number : 100001-581

Device Description : Spinal Jaxx OsteoSync 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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