Identity
- Trade Name
- Bone Hooks FDA UDI
- Generic Name
- Bone hook FDA UDI
- Device Name
- A hand-held, surgical instrument used for hooking around or into bone, typically to grasp, hold, and apply traction to the bone during a surgical intervention. It is a shaft-like instrument with a robust design and can have a singular hook or multiple hooks at the distal end and a handle of various designs at the proximal end. It is made of high-grade stainless steel. It is sometimes called a bone retractor. This is a reusable device. FDA UDI
- Model / Reference
- 12-081-20 FDA UDI
- Description
- A hand-held, surgical instrument used for hooking around or into bone, typically to grasp, hold, and apply traction to the bone during a surgical intervention. It is a shaft-like instrument with a robust design and can have a singular hook or multiple hooks at the distal end and a handle of various designs at the proximal end. It is made of high-grade stainless steel. It is sometimes called a bone retractor. This is a reusable device. FDA UDI
Identifiers
- Catalog Number
- 12-081-20 FDA UDI
- Primary DI / UDI-DI
- G25012081200 FDA UDI
- FDA Product Code
- KIK FDA UDI
- GMDN Term
- Bone hook FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 20 Centimeter FDA UDI
Category: Bone hook
Bone Hooks by N S Surgical Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone hook.
- RETRACTOR — KLS-Martin L.P. · Class I
- LEVER — KLS-Martin L.P. · Class I
- AESCULAP — AESCULAP, INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Novo Surgical Inc — NOVO SURGICAL, INC. · Class I
- AESCULAP — AESCULAP, INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- GELPI NEROMA RETRACTOR — SONTEC INSTRUMENTS, INC. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- N S Surgical Company
Sources (1)
- FDA UDI 7ff8c5e3-a9ea-4e48-ad7b-acb2f314cb80 35 fields · synced May 30, 2026