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)

MODEL 668, TRACTION SPLINT, ADULT

K-Number: K864765 · 1986-12-17

Decision Date1986-12-17
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODEL 668, TRACTION SPLINT, ADULT is the device name listed in this FDA 510(k) record. The listed applicant is Ferno-Washington, Inc.. It received FDA 510(k) clearance on 1986-12-17 under 510(k) number K864765. 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 MODEL 668, TRACTION SPLINT, ADULT?

MODEL 668, TRACTION SPLINT, ADULT is a medical device that received FDA 510(k) clearance on 1986-12-17. The listed applicant is Ferno-Washington, Inc.. The 510(k) number is K864765.

When did MODEL 668, TRACTION SPLINT, ADULT receive FDA 510(k) clearance?

MODEL 668, TRACTION SPLINT, ADULT received FDA 510(k) clearance on 1986-12-17, under 510(k) number K864765.

Who is the listed applicant for MODEL 668, TRACTION SPLINT, ADULT?

The FDA 510(k) record lists Ferno-Washington, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 668, TRACTION SPLINT, ADULT?

The FDA product code for MODEL 668, TRACTION SPLINT, ADULT 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.

Other records listing Ferno-Washington, Inc. 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: 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.

↑