Identity
- Trade Name
- Solar™ Interbody Fusion System FDA UDI
- Generic Name
- Surgical drill guide, reusable FDA UDI
- Device Name
- Solar™ 13mm Drill Guide FDA UDI
- Model / Reference
- 12-31N13 FDA UDI
- Description
- Solar™ 13mm Drill Guide FDA UDI
Identifiers
- Catalog Number
- 12-31N13 FDA UDI
- Primary DI / UDI-DI
- 00842048155010 FDA UDI
- 510(k) Number
- K231199 FDA UDI
- FDA Product Code
- OVD FDA UDIMAX FDA UDIPHM FDA UDI
- GMDN Term
- Surgical drill guide, reusable 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
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
Category: Surgical drill guide, reusable
Solar™ Interbody Fusion System by Degen Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical drill guide, reusable.
- ORTHOFIX — Orthofix, Inc. · Class I
- Titan™ — Ascension Orthopedics, Inc. · Class I
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class I
- Distal Elbow Plating System — SKELETAL DYNAMICS L.L.C. · Class II
- Truliant — Exactech, Inc. · Class II
- Vantage — Exactech, Inc. · Class II
- Legion — Smith & Nephew, Inc. · Class II
- Hintermann Series — Dt Medtech, LLC · Class I
Cleared under the same submission
K231199 also covers:
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
- Solar™ Interbody Fusion System — Degen Medical
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
- Degen Medical
Sources (1)
- FDA UDI 7a249ba8-d9b9-430a-a5d6-b8268535e7bd 37 fields · synced May 31, 2026