Identity
- Trade Name
- KASILOF Cervical Plate System FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
- Device Name
- KASILOF Cervical Plate 1 Level 33mm FDA UDI
- Model / Reference
- KCP1-133 FDA UDI
- Description
- KASILOF Cervical Plate 1 Level 33mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- B644KCP11330 FDA UDI
- 510(k) Number
- K173867 FDA UDI
- FDA Product Code
- KWQ FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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-screw internal spinal fixation system, non-sterile
KASILOF Cervical Plate System by Kahtnu Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone-screw internal spinal fixation system, non-sterile.
- TIGER Spine System — CORELINK LLC · Class II
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
- SILVERTON SPINAL FIXATION SYSTEM — BIOMET SPINE LLC · Class II
- POLARIS™ 5.5 SPINAL SYSTEM — BIOMET SPINE LLC · Class II
- Vitality® — BIOMET SPINE LLC · Class II
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
- PASS LP — Medicrea International SA · Class II
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
Cleared under the same submission
K173867 also covers:
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, Inc.
- KASILOF Cervical Plate System — Kahtnu Surgical, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Kahtnu Surgical, Inc.
Sources (1)
- FDA UDI edb39335-e6eb-41bb-803f-f5e6db54d279 34 fields · synced May 30, 2026