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FDA 510(k)

TRACTION UNITS

K-Number: K780228 · 1978-02-23

ApplicantBiomet, Inc.
Decision Date1978-02-23
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRACTION UNITS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1978-02-23 under 510(k) number K780228. 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 UNITS?

TRACTION UNITS is a medical device that received FDA 510(k) clearance on 1978-02-23. The listed applicant is Biomet, Inc.. The 510(k) number is K780228.

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

TRACTION UNITS received FDA 510(k) clearance on 1978-02-23, under 510(k) number K780228.

Who is the listed applicant for TRACTION UNITS?

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

What is the FDA product code for TRACTION UNITS?

The FDA product code for TRACTION UNITS is HST.

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Other records listing Biomet, Inc. as applicant

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Related Devices (Code: HST)

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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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