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FDA 510(k)

MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE

K-Number: K990120 · 1999-02-01

ApplicantDepuy Ace Medical Co.
Decision Date1999-02-01
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE 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 1999-02-01 under 510(k) number K990120. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE?

MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE is a medical device that received FDA 510(k) clearance on 1999-02-01. The listed applicant is Depuy Ace Medical Co.. The 510(k) number is K990120.

When did MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE receive FDA 510(k) clearance?

MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE received FDA 510(k) clearance on 1999-02-01, under 510(k) number K990120.

Who is the listed applicant for MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE?

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 MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE?

The FDA product code for MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE is HSB.

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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 PLATEK984458DEPUY ACE SPIDER PLATEK983853DEPUY ACE TIMAX META PLATEK983265DEPUY ACE COMPOSITE LOCKING NUTK982347DEPUY ACE TIMAX PILON PLATEK981775DEPUY ACE TIMAX CALCANEAL PERI-ARTICULAR PLATE

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Related Devices (Code: HSB)

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.

K261345Pediatric Nailing Platform FemurOrthoPediatrics Corp.K261481Pangea Femur Reconstruction SystemStryker GmbHK253080AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02)Suzhou and Science & Technology Development Corp.K261651Precice™ Max System and Precice™ Ankle Salvage SystemNuVasive Specialized OrthopedicsK253155Fule Metallic Lockable Intramedullary Nail SystemsBeijing Fule Science & Technology Development Co., Ltd.K253046HERA Interlocking Intramedullary Nailing SystemZheJiang Decans Medical Devices Co., Ltd.

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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