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FDA 510(k)

BONE SCREW WASHER

K-Number: K943782 · 1994-12-20

ApplicantAcu Med, Inc.
Decision Date1994-12-20
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BONE SCREW WASHER is the device name listed in this FDA 510(k) record. The listed applicant is Acu Med, Inc.. It received FDA 510(k) clearance on 1994-12-20 under 510(k) number K943782. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE SCREW WASHER?

BONE SCREW WASHER is a medical device that received FDA 510(k) clearance on 1994-12-20. The listed applicant is Acu Med, Inc.. The 510(k) number is K943782.

When did BONE SCREW WASHER receive FDA 510(k) clearance?

BONE SCREW WASHER received FDA 510(k) clearance on 1994-12-20, under 510(k) number K943782.

Who is the listed applicant for BONE SCREW WASHER?

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

What is the FDA product code for BONE SCREW WASHER?

The FDA product code for BONE SCREW WASHER is HTN.

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Other records listing Acu Med, Inc. as applicant

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.

K021321WRIST FUSION PLATEK013616POLARUS CAP SCREWK012655CONGRUENT BONE PLATE SYSTEMK992525ACUMED MODULAR SHOULDER SYSTEMK993657ACUMED SUTURE ANCHORK980103ACUMED SUTURE ANCHOR

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Related Devices (Code: HTN)

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.

K253115LARS ACJMovmedix S.A.S.K252081SportLinc Syndesmosis DeviceLincotek MedicalK253727Syndesmosis TightRope PROArthrex, Inc.K251643Synchfix EVTWright Medical Technology, Inc. (Stryker Corporation)K251134RipCordTriMed, Inc.K243624Acu-Sinch Knotless MiniAcumed, LLC

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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