Identity
- Trade Name
- IdentiTi II FDA UDI
- Generic Name
- Metallic spinal interbody fusion cage FDA UDI
- Device Name
- IdentiTi II LIF 10 x 22 x 60 mm, 10° FDA UDI
- Model / Reference
- 800-10226010-S FDA UDI
- Description
- IdentiTi II LIF 10 x 22 x 60 mm, 10° FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190376647791 FDA UDI
- 510(k) Number
- K242364 FDA UDI
- FDA Product Code
- PHM FDA UDIMAX FDA UDIOVD FDA UDI
- GMDN Term
- Metallic 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
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Height — 10 Millimeter FDA UDIAngle — 10 degree FDA UDILength — 60 Millimeter FDA UDIWidth — 22 Millimeter FDA UDI
Category: Metallic spinal interbody fusion cage
IdentiTi II by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metallic spinal interbody fusion cage.
- KODIAK CERVICAL IMPLANT, 14x16mm, 10mmx6° — MET 1 TECHNOLOGIES, LLC · Class II
- Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
- CoRoent — Nuvasive, Inc. · Class II
- Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
- MectaLIF 3D — Medacta International · Class II
- PILLAR TL — Orthofix US LLC · Class II
- Solar™ Interbody Fusion System — Degen Medical · Class II
- Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
Cleared under the same submission
K242364 also covers:
- AMP II — ALPHATEC SPINE, INC.
- AMP II — ALPHATEC SPINE, INC.
- AMP II — ALPHATEC SPINE, INC.
- AMP II — ALPHATEC SPINE, INC.
- AMP II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, INC.
- IdentiTi II — ALPHATEC SPINE, 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
- Alphatec Spine, Inc.
Sources (1)
- FDA UDI 314a118d-af21-4aab-a108-e3d0527e982a 36 fields · synced Jun 8, 2026