Identity
- Trade Name
- Paramount™ Anterior Cervical Spine System FDA UDI
- Generic Name
- Polymeric spinal interbody fusion cage FDA UDI
- Device Name
- Lordotic Scoring Trial, 10 mm x 14 mm x 13 mm FDA UDI
- Model / Reference
- 10-5604 FDA UDI
- Description
- Lordotic Scoring Trial, 10 mm x 14 mm x 13 mm FDA UDI
Identifiers
- Catalog Number
- 10-5604 FDA UDI
- Primary DI / UDI-DI
- 10840642111828 FDA UDI
- 510(k) Number
- K162760 FDA UDI
- FDA Product Code
- OVE FDA UDI
- GMDN Term
- Polymeric 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
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
Paramount™ Anterior Cervical Spine System by Spine Wave, 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
K162760 also covers:
- Paramount® Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, Inc.
- Paramount™ Anterior Cervical Spine System — Spine Wave, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Spine Wave, Inc.
Sources (1)
- FDA UDI 81dfb1a4-139e-4940-9662-2588ab6ae6a6 35 fields · synced May 30, 2026