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Streamline

FDA UDI

Class II (US FDA UDI)

by Surgalign Spine Technologies

Identity

Trade Name
Streamline FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
NAV TL DOUBLE LEAD TAP 4.5MM (D) FDA UDI
Model / Reference
02-TAP-45-MDN FDA UDI
Description
NAV TL DOUBLE LEAD TAP 4.5MM (D) FDA UDI

Identifiers

Primary DI / UDI-DI
00810076560335 FDA UDI
510(k) Number
K200095 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Bone tap, reusable 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone tap, reusable

Streamline by Surgalign Spine Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4e8b92f4-a7db-47e2-851f-b62365f7f9de 35 fields · synced Jun 1, 2026