Identity
- Trade Name
- Cortera FDA UDI
- Generic Name
- Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
- Device Name
- Probe, NAV, Lenke, Lumbar, Straight FDA UDI
- Model / Reference
- 1505-800240 FDA UDI
- Description
- Probe, NAV, Lenke, Lumbar, Straight FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840311232529 FDA UDI
- 510(k) Number
- K200095 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 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: Abdominal/ENT/orthopaedic surgical probe, reusable
Cortera by Surgalign Spine Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Abdominal/ENT/orthopaedic surgical probe, reusable.
- DRM Thoracic Pedicle Feeler 1 — Captiva Spine · Class I
- Medtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class I
- ISOLA — Depuy Spine, Inc. · Class I
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class I
- Invictus — ALPHATEC SPINE, INC. · Class I
- Optima™ Spinal System — CG MedTech Co., Ltd. · Class I
- General Instruments — ALPHATEC SPINE, INC. · Class I
- Medtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class I
Cleared under the same submission
K200095 also covers:
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
- Cortera — Surgalign Spine Technologies
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
- Surgalign Spine Technologies
Sources (1)
- FDA UDI 516397ff-c261-4c63-af1c-637ce6961e12 35 fields · synced May 30, 2026