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FDA 510(k)

EffortMed PEEK Cages & Corpectomy Cages

K-Number: K252686 · 2025-11-21

Decision Date2025-11-21
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EffortMed PEEK Cages & Corpectomy Cages is the device name listed in this FDA 510(k) record. The listed applicant is Effortmed, LLC. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K252686. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EffortMed PEEK Cages & Corpectomy Cages?

EffortMed PEEK Cages & Corpectomy Cages is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Effortmed, LLC. The 510(k) number is K252686.

When did EffortMed PEEK Cages & Corpectomy Cages receive FDA 510(k) clearance?

EffortMed PEEK Cages & Corpectomy Cages received FDA 510(k) clearance on 2025-11-21, under 510(k) number K252686.

Who is the listed applicant for EffortMed PEEK Cages & Corpectomy Cages?

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

What is the FDA product code for EffortMed PEEK Cages & Corpectomy Cages?

The FDA product code for EffortMed PEEK Cages & Corpectomy Cages is ODP.

Other records listing Effortmed, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: ODP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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