Identity
- Trade Name
- Ring Nut Loading Base FDA UDI
- Generic Name
- Orthopaedic implant aiming/guiding block attachment tool FDA UDI
- Model / Reference
- 88668 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290115932485 FDA UDI
- 510(k) Number
- K232719 FDA UDI
- FDA Product Code
- NKB FDA UDI
- GMDN Term
- Orthopaedic implant aiming/guiding block attachment tool FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 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: Orthopaedic implant aiming/guiding block attachment tool
Ring Nut Loading Base by Premia Spine Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K232719 also covers:
- Compressor — PREMIA SPINE LTD
- Distractor — PREMIA SPINE LTD
- PER System 50 — PREMIA SPINE LTD
- PER System 60 — PREMIA SPINE LTD
- PER System 75 — PREMIA SPINE LTD
- Rod Holding Forceps Self Retaining — PREMIA SPINE LTD
- Rod Length Measurement Tool — PREMIA SPINE LTD
- Rod Pusher — PREMIA SPINE LTD
- VersaLink Torque Limiter — PREMIA SPINE LTD
- Versalink Nut Counter Torque — PREMIA SPINE LTD
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
- Premia Spine Ltd
Sources (1)
- FDA UDI 37bd4323-ccf1-4bd7-a5ff-bb74902f68b7 33 fields · synced May 31, 2026