Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MOD-C

K-Number: K242303 · 2026-04-01

ApplicantOrthomod, LLC
Decision Date2026-04-01
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOD-C is a medical device manufactured by Orthomod, LLC. It received FDA 510(k) clearance on 2026-04-01 under approval number K242303. 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 MOD-C?

MOD-C is a medical device that received FDA 510(k) clearance on 2026-04-01. It is manufactured by Orthomod, LLC. The 510(k) number is K242303.

When was MOD-C approved by the FDA?

MOD-C received FDA 510(k) clearance on 2026-04-01, under approval number K242303.

What company makes MOD-C?

MOD-C is manufactured by Orthomod, LLC.

What is the FDA product code for MOD-C?

The FDA product code for MOD-C is ODP.

Related Devices (Code: ODP)

K161127The Small PLATEAU (PLATEAU-C) Spacer SystemLife Spine, Inc. K162003IMSE Cervical CageThe Institute of Musculoskeletal Science & Education K160222OIC Cervical PEEK SpacerThe Orthopaedic Implant Company K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageDio Medical Co., Ltd. K161649Virtu C Spinal Implant SystemMet 1 Technologies, LLC

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.

↑