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)

CERVITRAC TRACTION FRAME & CORD

K-Number: K821522 · 1982-06-21

Decision Date1982-06-21
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CERVITRAC TRACTION FRAME & CORD is the device name listed in this FDA 510(k) record. The listed applicant is George W. Cottrell. It received FDA 510(k) clearance on 1982-06-21 under 510(k) number K821522. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVITRAC TRACTION FRAME & CORD?

CERVITRAC TRACTION FRAME & CORD is a medical device that received FDA 510(k) clearance on 1982-06-21. The listed applicant is George W. Cottrell. The 510(k) number is K821522.

When did CERVITRAC TRACTION FRAME & CORD receive FDA 510(k) clearance?

CERVITRAC TRACTION FRAME & CORD received FDA 510(k) clearance on 1982-06-21, under 510(k) number K821522.

Who is the listed applicant for CERVITRAC TRACTION FRAME & CORD?

The FDA 510(k) record lists George W. Cottrell as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERVITRAC TRACTION FRAME & CORD?

The FDA product code for CERVITRAC TRACTION FRAME & CORD is HST.

Related Clinical Trials

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: HST)

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.

↑