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FDA 510(k)

DEPUY ACE COMPOSITE LOCKING NUT

K-Number: K983265 · 1998-10-26

ApplicantDepuy Ace Medical Co.
Decision Date1998-10-26
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY ACE COMPOSITE LOCKING NUT is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Ace Medical Co.. It received FDA 510(k) clearance on 1998-10-26 under 510(k) number K983265. 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 DEPUY ACE COMPOSITE LOCKING NUT?

DEPUY ACE COMPOSITE LOCKING NUT is a medical device that received FDA 510(k) clearance on 1998-10-26. The listed applicant is Depuy Ace Medical Co.. The 510(k) number is K983265.

When did DEPUY ACE COMPOSITE LOCKING NUT receive FDA 510(k) clearance?

DEPUY ACE COMPOSITE LOCKING NUT received FDA 510(k) clearance on 1998-10-26, under 510(k) number K983265.

Who is the listed applicant for DEPUY ACE COMPOSITE LOCKING NUT?

The FDA 510(k) record lists Depuy Ace Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEPUY ACE COMPOSITE LOCKING NUT?

The FDA product code for DEPUY ACE COMPOSITE LOCKING NUT is HTN.

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Other records listing Depuy Ace Medical Co. 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.

K990392DEPUY ACE SPIDER PLATEK990120MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATEK984458DEPUY ACE SPIDER PLATEK983853DEPUY ACE TIMAX META PLATEK982347DEPUY ACE TIMAX PILON PLATEK981775DEPUY ACE TIMAX CALCANEAL PERI-ARTICULAR PLATE

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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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