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Altus Spine

Last updated May 23, 2026

What Altus Spine makes

Altus Spine manufactures spinal implants and orthopaedic fixation devices, including non-bioabsorbable bone screws, metallic and polymeric interbody fusion cages, spinal fixation plates, and internal spinal fixation rods. Their portfolio also includes spinal implant trial systems, reusable orthopaedic surgical procedure kits, and internal spinal distractors for surgical procedures.

The company’s devices are classified under FDA categories Class I and Class II, with listings in the FDA’s Unique Device Identifier (UDI) database. Altus Spine is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Altus Spine manufacture?

Altus Spine specializes in spinal implants and orthopaedic fixation devices. Their product portfolio includes non-bioabsorbable bone screws, metallic and polymeric interbody fusion cages, spinal fixation plates, internal spinal fixation rods, spinal implant trial systems, reusable orthopaedic surgical procedure kits, and internal spinal distractors. These devices are designed for spinal surgeries and orthopaedic procedures.

Where is Altus Spine based?

Altus Spine is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with U.S. medical device regulations.

Which regulatory registries list Altus Spine’s devices?

Altus Spine’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare system.

How are Altus Spine’s devices classified under FDA regulations?

Altus Spine’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. Classification depends on factors like the device’s intended use and potential health impact.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: —
LinkedIn: —
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (5998)

Page 93 of 120

Device	Model / Reference	Registries	Class	Status
Brickyard Stand-Alone ALIF	SL32240813T	FDA UDI	Class II	Active
Brickyard ALIF	1020-42301213	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9620HA	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR124	FDA UDI	Class II	Active
Indy	1020-38270812	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP261008T	FDA UDI	Class II	Active
Indy	FA32241616T	FDA UDI	Class II	Active
Sochi	A10-24-1130	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-2120A	FDA UDI	Class I	Active
Brickyard Stand-Alone ALIF	SL38271619T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301614T	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SEC00932-12	FDA UDI	Class II	Active
Indy	FA34260818T	FDA UDI	Class II	Active
Pedicle Screw System	900-1044	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-5070	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-2212	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13050-12T	FDA UDI	Class II	Active
Indy	1030-38270813	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-4415	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730511T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8535	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	245-1005	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-9550	FDA UDI	Class II	Active
Monaco Uni-Planar	813-4555	FDA UDI	Class II	Active
Indy	FA38271219	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6145	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-5220	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38272518	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5165	FDA UDI	Class II	Active
Indy Standalone	SL42300819	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82816T2	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-6530	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-1009	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-7545	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5160	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38271219	FDA UDI	Class II	Active
Brickyard ALIF	FA32242013T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5035	FDA UDI	Class II	Active
Indy	1020-38271617	FDA UDI	Class II	Active
Indy	FA38271615T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S411011	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12250-14T	FDA UDI	Class II	Active
Fuji Cervical Plate System	121-4320	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8530	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-7530	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP301009	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	900-1017	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12255-12	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	245-1004	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8590	FDA UDI	Class II	Active

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