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FDA 510(k)

TRACTION ACCESSORIES

K-Number: K830244 · 1983-03-09

Decision Date1983-03-09
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRACTION ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Warm & Form, Orthopedic Materials. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830244. 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 TRACTION ACCESSORIES?

TRACTION ACCESSORIES is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Warm & Form, Orthopedic Materials. The 510(k) number is K830244.

When did TRACTION ACCESSORIES receive FDA 510(k) clearance?

TRACTION ACCESSORIES received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830244.

Who is the listed applicant for TRACTION ACCESSORIES?

The FDA 510(k) record lists Warm & Form, Orthopedic Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRACTION ACCESSORIES?

The FDA product code for TRACTION ACCESSORIES 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 Warm & Form, Orthopedic Materials 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.

View all 24 devices →

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.

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