Identity
- Trade Name
- ATEC Lateral Navigation Disc Prep Instruments FDA UDI
- Generic Name
- Surgical implant/trial-implant/sizer holder, reusable FDA UDI
- Device Name
- LIF NAV TRIAL 6 x 18 x 65 mm 10° FDA UDI
- Model / Reference
- 266-10-06186510-N FDA UDI
- Description
- LIF NAV TRIAL 6 x 18 x 65 mm 10° FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190376477107 FDA UDI
- 510(k) Number
- K223765 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
- Angle — 10 degree FDA UDILength — 65 Millimeter FDA UDIHeight — 6 Millimeter FDA UDIWidth — 18 Millimeter FDA UDI
Category: Surgical implant/trial-implant/sizer holder, reusable
ATEC Lateral Navigation Disc Prep Instruments by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical implant/trial-implant/sizer holder, reusable.
- Medtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- ARx — Life Spine, Inc. · Class II
- APEX 3D Total Ankle Replacement System — Paragon 28 · Class II
- JULIET INSTRUMENTATION — Spineart · Class II
- JOURNEY II XR — Smith & Nephew, Inc. · Class II
- TALOS® (HA) IBF — MEDITECH SPINE, LLC · Class II
- BENCOX THR System — Corentec Co., Ltd · Class II
Cleared under the same submission
K223765 also covers:
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — ALPHATEC SPINE, INC.
- ATEC Lateral Navigation Disc Prep Instruments — 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 393f918e-2882-4170-9525-5e1798a3393c 36 fields · synced Jun 8, 2026