Identity
- Trade Name
- MESA® Small Stature Spinal System FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system connector FDA UDI
- Device Name
- Transverse Connector, Semi- Adjustable Size 23 mm MESA Rail™-Rod FDA UDI
- Model / Reference
- 3001-70023AH FDA UDI
- Description
- Transverse Connector, Semi- Adjustable Size 23 mm MESA Rail™-Rod FDA UDI
Identifiers
- Catalog Number
- 3001-70023AH FDA UDI
- Primary DI / UDI-DI
- 10888857051102 FDA UDI
- FDA Product Code
- MNH FDA UDINKB FDA UDIOSH FDA UDIMNI FDA UDIKWP FDA UDIKWQ FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system connector 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
- Length — 23 Millimeter FDA UDIOuter Diameter — 4.5 Millimeter FDA UDI
Category: Bone-screw internal spinal fixation system connector
MESA® Small Stature Spinal System by K2m, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bone-screw internal spinal fixation system connector.
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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 bf20f4c9-e9fb-4fbb-873d-9a14df0b73ca 36 fields · synced May 30, 2026