Identity
- Trade Name
- ASTRA-OCT Spine System FDA UDI
- Generic Name
- Orthopaedic bone screw (non-sliding) FDA UDI
- Device Name
- ASTRA-OCT Dia.5.0mm Occipital Bone Screw, 14mm FDA UDI
- Model / Reference
- A3OS-5014 FDA UDI
- Description
- ASTRA-OCT Dia.5.0mm Occipital Bone Screw, 14mm FDA UDI
Identifiers
- Catalog Number
- A3OS-5014 FDA UDI
- Primary DI / UDI-DI
- 00193082110993 FDA UDI
- 510(k) Number
- K181350 FDA UDI
- FDA Product Code
- KWP FDA UDINKG FDA UDI
- GMDN Term
- Orthopaedic bone screw (non-sliding) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3050 FDA UDI888.3075 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
Category: Orthopaedic bone screw (non-sliding)
ASTRA-OCT Spine System by Spinecraft Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bone screw (non-sliding).
- EVOS — Smith & Nephew, Inc. · Class II
- TriLeap Lower Extremity Anatomic Plating System — CROSSROADS EXTREMITY SYSTEMS LLC · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Zavation — ZAVATION · Class II
- STARDRIVE — Synthes GmbH · Class IIb
- Arthrex® — Arthrex, Inc. · Class II
- Cancellous Screw, Locking — I.T.S. GmbH · Class II
- PANGEA — Stryker Corp. · Class II
Cleared under the same submission
K181350 also covers:
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
- ASTRA-OCT Spine System — SPINECRAFT LLC
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
- Spinecraft Llc
Sources (1)
- FDA UDI b9921029-c9d6-4f3e-b0a3-0f39c3bb250d 36 fields · synced May 31, 2026