Identity
- Trade Name
- A-CIFT FDA UDI
- Generic Name
- Polymeric spinal interbody fusion cage FDA UDI
- Device Name
- A-CIFT TRIAL HEADS, 14x 17, 10°, 5MM FDA UDI
- Model / Reference
- 14-32119-1005 FDA UDI
- Description
- A-CIFT TRIAL HEADS, 14x 17, 10°, 5MM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190361027645 FDA UDI
- 510(k) Number
- K131880 FDA UDI
- FDA Product Code
- OVE 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
No
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
- Width — 17 Millimeter FDA UDIAngle — 10 degree FDA UDIHeight — 5 Millimeter FDA UDILength — 13.5 Millimeter FDA UDI
Category: Polymeric spinal interbody fusion cage
A-Cift by Spinefrontier, Inc. — 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
- 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
- Peridot Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
Cleared under the same submission
K131880 also covers:
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — SPINEFRONTIER, INC.
- A-CIFT — 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 03d06dfa-0b4d-4f8f-83a9-29f98cbc4092 36 fields · synced Jun 6, 2026