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FDA 510(k)

SHAVER BLADE SET

K-Number: K940075 · 1994-04-15

ApplicantArthrex, Inc.
Decision Date1994-04-15
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SHAVER BLADE SET is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 1994-04-15 under 510(k) number K940075. 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 SHAVER BLADE SET?

SHAVER BLADE SET is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Arthrex, Inc.. The 510(k) number is K940075.

When did SHAVER BLADE SET receive FDA 510(k) clearance?

SHAVER BLADE SET received FDA 510(k) clearance on 1994-04-15, under 510(k) number K940075.

Who is the listed applicant for SHAVER BLADE SET?

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

What is the FDA product code for SHAVER BLADE SET?

The FDA product code for SHAVER BLADE SET is HRX.

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Other records listing Arthrex, Inc. as applicant

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Related Devices (Code: HRX)

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.

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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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