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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: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (5998)

Page 19 of 120

Device	Model / Reference	Registries	Class	Status
Brickyard Stand-Alone ALIF	SL38271613	FDA UDI	Class II	Active
Indy	1030-42301219	FDA UDI	Class II	Active
Brickyard	1030-0816	FDA UDI	Class I	Active
Sochi	A16-13-4026	FDA UDI	Class II	Active
Indy	FA38272019T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	730-0014	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-6100	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0477	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP221006T2	FDA UDI	Class II	Active
Brickyard	1020-42301218	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F11855-10T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-9540	FDA UDI	Class II	Active
Fuji Cervical Plate System	138-4312	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-7600	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-8590	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02260-08T	FDA UDI	Class II	Active
Indy Standalone	SL32242518	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730008T	FDA UDI	Class II	Active
Brickyard	1030-42302019	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301213	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP221018	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8555	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	905-0048	FDA UDI	Class II	Active
Fuji Cervical Plate System	122-4016	FDA UDI	Class II	Active
Brickyard	1030-1214	FDA UDI	Class I	Active
Altus Spine Pedicle Screw System	880-1026L	FDA UDI	Class II	Active
Indy	1030-0818	FDA UDI	Class I	Active
Silverstone Titanium Interbody Fusion System	ST83214T2	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38270811T	FDA UDI	Class II	Active
Brickyard	1020-38271619	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9545HA	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-221009	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-7560	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP261016T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-6565	FDA UDI	Class II	Active
Indy	FA34262515	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420509	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9580HA	FDA UDI	Class II	Active
Monaco Uni-Planar	811-6060	FDA UDI	Class II	Active
Brickyard ALIF	FA38270817T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-8550	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	942-5400	FDA UDI	Class II	Active
Indy	FA32241217T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-3013	FDA UDI	Class I	Active
Indy Standalone	SL42301218	FDA UDI	Class II	Active
Brickyard ALIF	FA32242020	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP301012T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-5535	FDA UDI	Class II	Active
Brickyard ALIF	FA34261614T	FDA UDI	Class II	Active
Fuji Cervical Plate System	121-4318	FDA UDI	Class II	Active

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