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FDA 510(k)

ARTHTOTEK PRECISION HAND INSTRUMENTATION

K-Number: K933070 · 1994-03-24

ApplicantBiomet, Inc.
Decision Date1994-03-24
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHTOTEK PRECISION HAND INSTRUMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1994-03-24 under 510(k) number K933070. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHTOTEK PRECISION HAND INSTRUMENTATION?

ARTHTOTEK PRECISION HAND INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 1994-03-24. The listed applicant is Biomet, Inc.. The 510(k) number is K933070.

When did ARTHTOTEK PRECISION HAND INSTRUMENTATION receive FDA 510(k) clearance?

ARTHTOTEK PRECISION HAND INSTRUMENTATION received FDA 510(k) clearance on 1994-03-24, under 510(k) number K933070.

Who is the listed applicant for ARTHTOTEK PRECISION HAND INSTRUMENTATION?

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 ARTHTOTEK PRECISION HAND INSTRUMENTATION?

The FDA product code for ARTHTOTEK PRECISION HAND INSTRUMENTATION is HRX.

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Related Devices (Code: HRX)

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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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