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FDA 510(k)

Spinalogic Bone Growth Stimulator

K-Number: K262721 · 2026-09-29

ApplicantDjo, LLC
Decision Date2026-09-29
Product CodeLOF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Spinalogic Bone Growth Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Djo, LLC. It received FDA 510(k) clearance on 2026-09-29 under 510(k) number K262721. The device is classified under product code LOF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Spinalogic Bone Growth Stimulator?

Spinalogic Bone Growth Stimulator is a medical device that received FDA 510(k) clearance on 2026-09-29. The listed applicant is Djo, LLC. The 510(k) number is K262721.

When did Spinalogic Bone Growth Stimulator receive FDA 510(k) clearance?

Spinalogic Bone Growth Stimulator received FDA 510(k) clearance on 2026-09-29, under 510(k) number K262721.

Who is the listed applicant for Spinalogic Bone Growth Stimulator?

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

What is the FDA product code for Spinalogic Bone Growth Stimulator?

The FDA product code for Spinalogic Bone Growth Stimulator is LOF.

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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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