Identity
- Trade Name
- INTERBODY FUSION DEVICES FDA UDI
- Generic Name
- Polymeric spinal interbody fusion cage FDA UDI
- Device Name
- SHURFIT LLIF PEEK 22x60x12mm (qty 21) FDA UDI
- Model / Reference
- 11105PS FDA UDI
- Description
- SHURFIT LLIF PEEK 22x60x12mm (qty 21) FDA UDI
Identifiers
- Catalog Number
- 23-PC2260-12 FDA UDI
- Primary DI / UDI-DI
- 00815362023235 FDA UDI
- 510(k) Number
- K092193 FDA UDI
- FDA Product Code
- KWQ FDA UDIMAX FDA UDI
- GMDN Term
- Polymeric spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 FDA UDI888.3080 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: Polymeric spinal interbody fusion cage
Interbody Fusion Devices by Precision Spine, 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
- S-LIFT® — SPINEFRONTIER, 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
Cleared under the same submission
K092193 also covers:
- AccuFit RP System — Precision Spine, Inc.
- AccuFit RP System — Precision Spine, Inc.
- Intervertebral Body Fusion Device — Precision Spine, Inc.
- Intervertebral Body Fusion Device — Precision Spine, Inc.
- MD Vue Discectomy — Precision Spine, Inc.
- MD Vue Discectomy — Precision Spine, Inc.
- MD-Vue Lateral Access System — Precision Spine, Inc.
- MD-Vue™ Lateral Discectomy System — Precision Spine, Inc.
- MD-Vue™ Lateral Discectomy System — Precision Spine, Inc.
- MD-Vue™ Lateral Discectomy System — Precision Spine, Inc.
- ShurFit Interbody Device — Precision Spine, Inc.
- ShurFit Interbody Device — Precision 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
- Precision Spine, Inc.
Sources (1)
- FDA UDI 025e1fab-3e67-4255-b13e-4501d4761472 35 fields · synced Jun 1, 2026