PICASSO MIS Spinal System (UDI 016.3200)
Manufactured by CTL Medical Corporation
Device Regulatory Overview
The PICASSO MIS Spinal System (Model/Catalog Number: 016.3200) is a medical device manufactured by CTL Medical Corporation. This product is indexed under FDA Product Code / Category Classification NKB within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 016.3200
- Product Code / EMDN
- NKB
- Device Name
- Percutaneous Curved Rod D6.0 x 200mm
- Database Sync Date
- 2026-08-09 09:24:06
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PICASSO MIS Spinal System?
The registered manufacturer of record for PICASSO MIS Spinal System is CTL Medical Corporation.
What is the Primary UDI-DI identifier for PICASSO MIS Spinal System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 016.3200.
What classification code is assigned to this device?
This device is registered under product classification code NKB.
Similar Classification Devices (NKB)
Other Devices by CTL Medical Corporation
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