Identity
- Trade Name
- MESA® Spinal System FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system hook FDA UDI
- Device Name
- Angled Transverse Process Hook, Right Size 8 mm FDA UDI
- Model / Reference
- 801-80805H FDA UDI
- Description
- Angled Transverse Process Hook, Right Size 8 mm FDA UDI
Identifiers
- Catalog Number
- 801-80805H FDA UDI
- Primary DI / UDI-DI
- 10888857142800 FDA UDI
- FDA Product Code
- NKB FDA UDIOSH FDA UDIKWP FDA UDIMNI FDA UDIKWQ FDA UDIMNH FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system hook FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI888.3050 FDA UDI888.3060 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
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Depth — 8 Millimeter FDA UDILength — 8 Millimeter FDA UDIOuter Diameter — 5.5 Millimeter FDA UDIWidth — 7 Millimeter FDA UDI
Category: Bone-screw internal spinal fixation system hook
MESA® Spinal System by K2m, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone-screw internal spinal fixation system hook.
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- PASS LP PASS TL — Medicrea International SA · Class II
- TSRH® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
- ReLine — Nuvasive, Inc. · Class II
- COSY — SIGNUS Medizintechnik GmbH · Class II
- neon³™ OCT spinal stabilization — Ulrich GmbH & Co. KG · Class II
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
- K2m, Inc.
Sources (1)
- FDA UDI 32759f8f-30f9-4387-b4f6-3a5ef73d08b1 36 fields · synced May 30, 2026