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SNAP Mini Desktop

FDA UDI

Class II (US FDA UDI)

by Surgical Theater Llc

Identity

Trade Name
SNAP Mini Desktop FDA UDI
Generic Name
Surgical planning/navigation-enhancement system FDA UDI
Device Name
Surgical Navigation Advanced Platform (SNAP) Patient Engagement Desktop System FDA UDI
Model / Reference
VR MSNAP FDA UDI
Description
Surgical Navigation Advanced Platform (SNAP) Patient Engagement Desktop System FDA UDI

Identifiers

Primary DI / UDI-DI
00863157000367 FDA UDI
510(k) Number
K160584 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Surgical planning/navigation-enhancement system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical planning/navigation-enhancement system

SNAP Mini Desktop by Surgical Theater Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical planning/navigation-enhancement system.

Cleared under the same submission

K160584 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgical Theater Llc

Sources (1)

  • FDA UDI c013eba0-742d-49ab-81f2-fe159dc13cdd 35 fields · synced May 29, 2026