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 a medical device manufactured by K2m, Inc.. It received FDA 510(k) clearance on 2026-02-06 under approval 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. It is manufactured by K2m, Inc.. The 510(k) number is K252873.
When was Q Interbody Instruments approved by the FDA?
Q Interbody Instruments received FDA 510(k) clearance on 2026-02-06, under approval number K252873.
What company makes Q Interbody Instruments?
Q Interbody Instruments is manufactured by K2m, Inc..
What is the FDA product code for Q Interbody Instruments?
The FDA product code for Q Interbody Instruments is 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.