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 - 00818956020009 Catalog Number : 100001-501

Device Description : Spinal Jaxx Implant, 7Hx10Wx21L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020016 Catalog Number : 100001-502

Device Description : Spinal Jaxx Implant, 7Hx12Wx21L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020023 Catalog Number : 100001-503

Device Description : Spinal Jaxx Implant, 7Hx10Wx25L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020030 Catalog Number : 100001-504

Device Description : Spinal Jaxx Implant, 7Hx12Wx25L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020047 Catalog Number : 100001-505

Device Description : Spinal Jaxx Implant, 7Hx10Wx29L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020054 Catalog Number : 100001-506

Device Description : Spinal Jaxx Implant, 7Hx12Wx29L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020061 Catalog Number : 100001-507

Device Description : Spinal Jaxx Implant, 7Hx10Wx33L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020078 Catalog Number : 100001-508

Device Description : Spinal Jaxx Implant, 7Hx12Wx33L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020085 Catalog Number : 100001-509

Device Description : Spinal Jaxx Implant, 9Hx10Wx21L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Spinal Jaxx Interbody Fusion Device - 00818956020092 Catalog Number : 100001-510

Device Description : Spinal Jaxx Implant, 9Hx12Wx21L mm

Device Class : 2

Duns Number: 080554344

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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