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

Q Interbody Instruments

K Number: K252873 · Decision Feb 6, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
100
Review Days
149

Basic Information

Device Name
Q Interbody Instruments
K Number
K252873
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
K2m, Inc.
Date Received
September 10, 2025
Decision Date
February 6, 2026
Product Code
OLO
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
OLO Orthopedic Stereotaxic Instrument

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