ADVANCED RESEARCH MEDICAL LLC

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

Want to know more about this Organization? Request more information now!

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) (5) Orthopedic Manual Surgical Instrument (LXH) (5)

Premarket Exempt

No Yes

Clear

N/A - 00840239800534 Catalog Number : B-20-1

Device Description : Decorticator - Dilator

Device Class : 1

Duns Number: 117201206

Premarket Exempt : Yes

Product Code : LXH

Prescription Use : Yes

Device Count : 1

N/A - 00840239800541 Catalog Number : B-20-2

Device Description : Decorticator

Device Class : 1

Duns Number: 117201206

Premarket Exempt : Yes

Product Code : LXH

Prescription Use : Yes

Device Count : 1

N/A - 00840239800558 Catalog Number : B-20-3

Device Description : Decorticator - Plunger

Device Class : 1

Duns Number: 117201206

Premarket Exempt : Yes

Product Code : LXH

Prescription Use : Yes

Device Count : 1

N/A - 00840239800565 Catalog Number : B-20-4

Device Description : Decorticator - Rasp

Device Class : 1

Duns Number: 117201206

Premarket Exempt : Yes

Product Code : LXH

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575007 Catalog Number : 01-2708

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique Implant 9.5 x 27 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) - 00850014575014 Catalog Number : 01-00-1

Device Description : Lumbar Interbody Fusion System (OLLIF) Inserter-Outer

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575021 Catalog Number : 01-2000

Device Description : Lumbar Interbody Fusion System (OLLIF) Instrument Set in Graphic Sterilization Case

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575038 Catalog Number : 01-2001

Device Description : Lumbar Interbody Fusion System (OLLIF) Instrument Set in Sterilization Case

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) Inserter- Outer - 00850014575045 Catalog Number : 01-00-2

Device Description : OLLIF Inserter-Inner

Device Class : 1

Duns Number: 117201206

Premarket Exempt : Yes

Product Code : LXH

Prescription Use : Yes

Device Count : 1

Lumbar Interbody Fusion System (OLLIF) - 00850014575069 Catalog Number : 01-2709

Device Description : Lumbar Interbody Fusion System (OLLIF) Oblique Implant 9.5 x 27 x 9 mm

Device Class : 2

Duns Number: 117201206

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Previous 1 … 4 5 6 … 12 Next