Identity
- Trade Name
- Indus® FDA UDI
- Generic Name
- Spinal fixation plate, non-bioabsorbable FDA UDI
- Device Name
- Invue Max, Four Level ACP, 89mm FDA UDI
- Model / Reference
- 01-71007-89 FDA UDI
- Description
- Invue Max, Four Level ACP, 89mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190361001508 FDA UDI
- 510(k) Number
- K121060 FDA UDI
- FDA Product Code
- KWQ FDA UDI
- GMDN Term
- Spinal fixation plate, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 89 Millimeter FDA UDIWidth — 16.5 Millimeter FDA UDI
Category: Spinal fixation plate, non-bioabsorbable
Indus® by Spinefrontier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal fixation plate, non-bioabsorbable.
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- TSLP — Synthes · Class II
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- PROVIDENCE — GLOBUS MEDICAL, INC. · Class II
- ACP — Nuvasive, Inc. · Class II
- uNion Cervical Plate System — ULRICH MEDICAL USA, INC. · Class II
Cleared under the same submission
K121060 also covers:
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
- Indus — SPINEFRONTIER, INC.
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 |
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Manufacturer
- Manufacturer
- Spinefrontier, Inc.
Sources (1)
- FDA UDI 218a98e1-1260-4bb4-af2e-553276ad619d 36 fields · synced Jun 8, 2026