Streamline TL Spinal Fixation System (UDI 01-PA-675-70)
Manufactured by Pioneer Surgical Technology, Inc.
Device Regulatory Overview
The Streamline TL Spinal Fixation System (Model/Catalog Number: 01-PA-675-70) is a medical device manufactured by Pioneer Surgical Technology, Inc.. This product is indexed under FDA Product Code / Category Classification NKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 01-PA-675-70
- Product Code / EMDN
- NKB
- Device Name
- PEDICLE SCREW, POLYAXIAL
- Database Sync Date
- 2026-08-09 09:02:16
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 Streamline TL Spinal Fixation System?
The registered manufacturer of record for Streamline TL Spinal Fixation System is Pioneer Surgical Technology, Inc..
What is the Primary UDI-DI identifier for Streamline TL Spinal Fixation System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01-PA-675-70.
What classification code is assigned to this device?
This device is registered under product classification code NKB.
Similar Classification Devices (NKB)
Other Devices by Pioneer Surgical Technology, Inc.
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