Identity
- Trade Name
- Arsenal Deformity Spinal Fixation System FDA UDI
- Generic Name
- Spinal bone screw, non-bioabsorbable FDA UDI
- Device Name
- ILIAC BOLT, 10 DEGREE, 9.0mm X 50mm FDA UDI
- Model / Reference
- 48700-010-090-050 FDA UDI
- Description
- ILIAC BOLT, 10 DEGREE, 9.0mm X 50mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840967113210 FDA UDI
- 510(k) Number
- K152968 FDA UDI
- FDA Product Code
- MNI FDA UDIKWP FDA UDIOSH FDA UDINKB FDA UDINMH FDA UDI
- GMDN Term
- Spinal bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI888.3050 FDA UDI884.1720 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
- Outer Diameter — 9 Millimeter FDA UDIAngle — 10 degree FDA UDILength — 50 Millimeter FDA UDI
Category: Spinal bone screw, non-bioabsorbable
Arsenal Deformity Spinal Fixation System by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spinal bone screw, non-bioabsorbable.
- 4CIS® Chiron Spinal Fixation System — ALPHANOX CO., LTD. · Class II
- LnK/PathLoc-L MIS Spinal System — L&K BIOMED CO. , LTD. · Class II
- ASPIRON™ ACPSYSTEM — CG MedTech Co., Ltd. · Class II
- Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
- OpenLoc-L Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
- Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
- AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
- Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · Class II
Cleared under the same submission
K152968 also covers:
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — ALPHATEC SPINE, INC.
- Arsenal Deformity Spinal Fixation System — 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 998ba969-f466-4a3a-88c1-f8b5b7c325b8 36 fields · synced Jun 8, 2026