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

FDA 510(k)

IMSE Cervical Cage

K-Number: K162003 · 2016-12-21

Decision Date2016-12-21
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IMSE Cervical Cage is the device name listed in this FDA 510(k) record. The listed applicant is The Institute of Musculoskeletal Science & Education. It received FDA 510(k) clearance on 2016-12-21 under 510(k) number K162003. 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 IMSE Cervical Cage?

IMSE Cervical Cage is a medical device that received FDA 510(k) clearance on 2016-12-21. The listed applicant is The Institute of Musculoskeletal Science & Education. The 510(k) number is K162003.

When did IMSE Cervical Cage receive FDA 510(k) clearance?

IMSE Cervical Cage received FDA 510(k) clearance on 2016-12-21, under 510(k) number K162003.

Who is the listed applicant for IMSE Cervical Cage?

The FDA 510(k) record lists The Institute of Musculoskeletal Science & Education as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMSE Cervical Cage?

The FDA product code for IMSE Cervical Cage is ODP.

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

View on FDA Database →

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