FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Packaged Assembly, Reusable Navigation Unit; Lantern ASC, Smart Pack kit, Knee

K Number: K253507 · Decision Jun 2, 2026
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
16
Applicant Total
14
Review Days
211

Basic Information

Device Name
Packaged Assembly, Reusable Navigation Unit; Lantern ASC, Smart Pack kit, Knee
K Number
K253507
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthalign, Inc.
Date Received
November 3, 2025
Decision Date
June 2, 2026
Product Code
ONN
Advisory Committee
Neurology
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ONN Intraoperative Orthopedic Joint Assessment Aid

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K162962 OrthAlign Plus System
K153237 OrthAlign Plus System
K140331 ORTHALIGN PLUS SYSTEM
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