Identity
- Trade Name
- Centerline Thoracolumbar Spinal System FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- Nautilus Gx Ø4.5 Tap - Non-Cannulated FDA UDI
- Model / Reference
- 176-014 FDA UDI
- Description
- Nautilus Gx Ø4.5 Tap - Non-Cannulated FDA UDI
Identifiers
- Catalog Number
- 176-014 FDA UDI
- Primary DI / UDI-DI
- 00190837064525 FDA UDI
- 510(k) Number
- K151196 FDA UDI
- FDA Product Code
- NKB FDA UDI
- GMDN Term
- Bone tap, reusable 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: Bone tap, reusable
Centerline Thoracolumbar Spinal System by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone tap, reusable.
- BIOSURE — Smith & Nephew, Inc. · Class I
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- CORTICAL TAP — Biomet Orthopedics, Inc. · Class I
- PressON™ — NEXUS SPINE, L.L.C. · Class I
- Insite — TORNIER, INC. · Class I
- ReLine — Nuvasive, Inc. · Class I
- Mariner MIS — SeaSpine Orthopedics Corporation · Class I
- Response 5.5/6.0 Spine System — ORTHOPEDIATRICS CORP. · Class I
Cleared under the same submission
K151196 also covers:
- Centerline — Life Spine, Inc.
- Centerline — Life Spine, Inc.
- Centerline — Life Spine, Inc.
- Centerline — Life Spine, Inc.
- Centerline — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
- Centerline Cannulated Accessories — Life Spine, Inc.
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
- Life Spine, Inc.
Sources (1)
- FDA UDI 4b1890bc-0ca4-4e10-b82a-bc6443e23376 35 fields · synced Jun 8, 2026