Identity
- Trade Name
- CoLink FDA UDI
- Generic Name
- Surgical drill guide, reusable FDA UDI
- Device Name
- MIS PLATE TARGETING GUIDE, KWIRE GUIDE FDA UDI
- Model / Reference
- P02 N0231 FDA UDI
- Description
- MIS PLATE TARGETING GUIDE, KWIRE GUIDE FDA UDI
Identifiers
- Catalog Number
- P02 N0231 FDA UDI
- Primary DI / UDI-DI
- 00810021869827 FDA UDI
- 510(k) Number
- K213069 FDA UDI
- FDA Product Code
- FZX FDA UDI
- GMDN Term
- Surgical drill guide, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Safe FDA UDI
Category: Surgical drill guide, reusable
CoLink by In2Bones, USA — Class I — 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
K213069 also covers:
- CoLink — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- CoLink® NeoFuse — In2Bones, USA
- In2Bones — In2Bones, USA
- In2Bones — In2Bones, USA
- In2Bones — In2Bones, USA
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- In2Bones, USA
Sources (1)
- FDA UDI 8e578fa4-a231-4f40-975b-d71287a319a9 36 fields · synced May 30, 2026