510(k) K243258

Device
Paradigm System
Applicant
Proprio, Inc.
510(k) number
K243258
Product code
OLO
Decision
Substantially Equivalent (SESE)
Decision date
2025-02-21
Date received
2024-10-15
Regulation
882.4560
Classification name
Orthopedic Stereotaxic Instrument
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Shannon Eubanks
Address
111 W. John St., Suite 308 Seattle WA US 98119 98119

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00850042604267ParadigmProprio, Inc.2025-03-21
00850042604229ParadigmProprio, Inc.2025-03-21
00850042604212ParadigmProprio, Inc.2025-03-21
00850042604205ParadigmProprio, Inc.2025-03-21
00850042604199ParadigmProprio, Inc.2025-03-21
00850042604182ParadigmProprio, Inc.2025-03-21
00850042604175ParadigmProprio, Inc.2025-03-21
00850042604168ParadigmProprio, Inc.2025-03-21
00850042604151ParadigmProprio, Inc.2025-03-21
00850042604144ParadigmProprio, Inc.2025-03-21
00850042604137ParadigmProprio, Inc.2025-03-21
00850042604120ParadigmProprio, Inc.2025-03-21
00850042604113ParadigmProprio, Inc.2025-03-21
00850042604021ParadigmProprio, Inc.2025-03-21
00850042604014ParadigmProprio, Inc.2025-03-21

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