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FDA 510(k)

Q Interbody Instruments

K-Number: K252873 · 2026-02-06

ApplicantK2m, Inc.
Decision Date2026-02-06
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Q Interbody Instruments is the device name listed in this FDA 510(k) record. The listed applicant is K2m, Inc.. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K252873. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q Interbody Instruments?

Q Interbody Instruments is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is K2m, Inc.. The 510(k) number is K252873.

When did Q Interbody Instruments receive FDA 510(k) clearance?

Q Interbody Instruments received FDA 510(k) clearance on 2026-02-06, under 510(k) number K252873.

Who is the listed applicant for Q Interbody Instruments?

The FDA 510(k) record lists K2m, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q Interbody Instruments?

The FDA product code for Q Interbody Instruments is OLO.

Other records listing K2m, Inc. as applicant

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Related Devices (Code: OLO)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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