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FDA 510(k)

BACKTRAC 90-90 TRACTION

K-Number: K802869 · 1980-12-11

ApplicantBacktrac
Decision Date1980-12-11
Product CodeKQZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BACKTRAC 90-90 TRACTION is the device name listed in this FDA 510(k) record. The listed applicant is Backtrac. It received FDA 510(k) clearance on 1980-12-11 under 510(k) number K802869. The device is classified under product code KQZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACKTRAC 90-90 TRACTION?

BACKTRAC 90-90 TRACTION is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Backtrac. The 510(k) number is K802869.

When did BACKTRAC 90-90 TRACTION receive FDA 510(k) clearance?

BACKTRAC 90-90 TRACTION received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802869.

Who is the listed applicant for BACKTRAC 90-90 TRACTION?

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

What is the FDA product code for BACKTRAC 90-90 TRACTION?

The FDA product code for BACKTRAC 90-90 TRACTION is KQZ.

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: KQZ)

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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