Identity
- Trade Name
- C-Clamp medium FDA UDI
- Generic Name
- Neurological stereotactic surgery system FDA UDI
- Device Name
- C-clamp medium for Navient FDA UDI
- Model / Reference
- 950-NE-UTCM FDA UDI
- Description
- C-clamp medium for Navient FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07540209956317 FDA UDI
- 510(k) Number
- K163439 FDA UDI
- FDA Product Code
- HAW FDA UDI
- GMDN Term
- Neurological stereotactic surgery system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Neurological stereotactic surgery system
C-Clamp medium by ClaroNav Kolahi Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Neurological stereotactic surgery system.
- Gauge for Softouch Registration Pointer — Brainlab SE · Class I
- PEEK INSTRUMENT ADAPTOR Ø2.15MM — MEDTECH LLC · Class II
- Mini-Bolt VUE Accessory Kit — MONTERIS MEDICAL CORP · Class I
- StealthAiR™ Spine — MEDTRONIC NAVIGATION, INC. · Class II
- StealthStation — MEDTRONIC NAVIGATION, INC. · Class II
- OsteoMed™ Manual Driver Handle — FHC, INC. · Class II
- PMT CORPORATION - STEREOTACTIC — Pmt Corp. · Class II
- Leksell Stereotactic System — Elekta Instrument AB · Class II
Cleared under the same submission
K163439 also covers:
- Bayonet Probe — ClaroNav Kolahi Inc
- Bayonet Probe — ClaroNav Kolahi Inc
- C-Clamp Large — ClaroNav Kolahi Inc
- C-Clamp XL — ClaroNav Kolahi Inc
- C-Clamp small — ClaroNav Kolahi Inc
- ENT Sterilization Tray — ClaroNav Kolahi Inc
- Frontal Seeker — ClaroNav Kolahi Inc
- Frontal Seeker B — ClaroNav Kolahi Inc
- Maxillary Seeker — ClaroNav Kolahi Inc
- Maxillary Seeker B — ClaroNav Kolahi Inc
- NaviENT — ClaroNav Kolahi Inc
- NaviENT Accessory Kit — ClaroNav Kolahi 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
- ClaroNav Kolahi Inc
Sources (1)
- FDA UDI d343fd46-a29b-4025-ae41-41db8f2755fb 34 fields · synced May 30, 2026