ADVANCED RESEARCH MEDICAL LLC

Address:1515 HIGHWAY 13 EAST,Burnsville,MN,55337,US

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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

No Yes

Clear

Lumbar Interbody Fusion System (OLLIF) - 00850014575281 Catalog Number : 01-3309

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique Implant 9.5 x 33 x 9 mm

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575298 Catalog Number : 01-3308

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique Implant 9.5 x 33 x 8 mm

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575311 Catalog Number : 01-06-4

Device Description : Lumbar Interbody Fusion System (OLLIF) Flexible Curette Loop Blade

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575328 Catalog Number : O-2700

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique 27 mm Implants in Caddy

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575335 Catalog Number : O-3000

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique 30 mm Implants in Caddy

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575342 Catalog Number : O-3300

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique 33 mm Implants in Caddy

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575359 Catalog Number : 01-01

Device Description : Lumbar Interbody Fusion System (OLLIF) Dilator

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575366 Catalog Number : 01-02

Device Description : Lumbar Interbody Fusion System (OLLIF) Access Portal

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575373 Catalog Number : 01-03

Device Description : Lumbar Interbody Fusion System (OLLIF) Disc Drill

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575380 Catalog Number : 01-04-1

Device Description : Lumbar Interbody Fusion System (OLLIF) Shaper - Body

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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