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FDA 510(k)

ARTHREX CIRCULAR HARVESTING SAW

K-Number: K941681 · 1994-08-25

ApplicantArthrex, Inc.
Decision Date1994-08-25
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHREX CIRCULAR HARVESTING SAW is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 1994-08-25 under 510(k) number K941681. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHREX CIRCULAR HARVESTING SAW?

ARTHREX CIRCULAR HARVESTING SAW is a medical device that received FDA 510(k) clearance on 1994-08-25. The listed applicant is Arthrex, Inc.. The 510(k) number is K941681.

When did ARTHREX CIRCULAR HARVESTING SAW receive FDA 510(k) clearance?

ARTHREX CIRCULAR HARVESTING SAW received FDA 510(k) clearance on 1994-08-25, under 510(k) number K941681.

Who is the listed applicant for ARTHREX CIRCULAR HARVESTING SAW?

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 ARTHREX CIRCULAR HARVESTING SAW?

The FDA product code for ARTHREX CIRCULAR HARVESTING SAW is HSZ.

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Other records listing Arthrex, Inc. as applicant

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Related Devices (Code: HSZ)

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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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