← Back to catalogue
Silverstone Titanium Interbody Fusion System
FDA UDIClass II (US FDA UDI)
by Altus Spine
Identity
- Trade Name
- Silverstone Titanium Interbody Fusion System FDA UDI
- Generic Name
- Polymeric spinal interbody fusion cage FDA UDI
- Device Name
- 22x10x10mm 5degree PEEK Silverstone-T FDA UDI
- Model / Reference
- ST52210 FDA UDI
- Description
- 22x10x10mm 5degree PEEK Silverstone-T FDA UDI
Identifiers
- Primary DI / UDI-DI
- B417ST522101 FDA UDI
- 510(k) Number
- K170512 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Polymeric spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 10 Millimeter FDA UDIHeight — 10 Millimeter FDA UDIAngle — 5 degree FDA UDILength — 22 Millimeter FDA UDI
Category: Polymeric spinal interbody fusion cage
Silverstone Titanium Interbody Fusion System by Altus Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polymeric spinal interbody fusion cage.
- L-Box® — Innovasis, Inc. · Class II
- CoRoent — Nuvasive, Inc. · Class II
- Novel Spinal Spacer System — ALPHATEC SPINE, INC. · Class II
- S-LIFT® — SPINEFRONTIER, INC. · Class II
- Peridot Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
- TAURUS PEEK Cage System — Medyssey Co., Ltd. · Class II
- Cross-Fuse® II PEEK IBF System — Rti Surgical, Inc. · Class II
- Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
Cleared under the same submission
K170512 also covers:
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
- Imola Titanium Interbody Fusion System — Altus Spine
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Altus Spine
Sources (1)
- FDA UDI dd00c37f-d124-4214-a7a5-ce545f4c2ba5 36 fields · synced May 31, 2026