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FDA 510(k)

TRANSFX MULTI PIN CLAMP

K-Number: K991723 · 1999-07-22

ApplicantImmedica, Inc.
Decision Date1999-07-22
Product CodeLXT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRANSFX MULTI PIN CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Immedica, Inc.. It received FDA 510(k) clearance on 1999-07-22 under 510(k) number K991723. The device is classified under product code LXT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSFX MULTI PIN CLAMP?

TRANSFX MULTI PIN CLAMP is a medical device that received FDA 510(k) clearance on 1999-07-22. The listed applicant is Immedica, Inc.. The 510(k) number is K991723.

When did TRANSFX MULTI PIN CLAMP receive FDA 510(k) clearance?

TRANSFX MULTI PIN CLAMP received FDA 510(k) clearance on 1999-07-22, under 510(k) number K991723.

Who is the listed applicant for TRANSFX MULTI PIN CLAMP?

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

What is the FDA product code for TRANSFX MULTI PIN CLAMP?

The FDA product code for TRANSFX MULTI PIN CLAMP is LXT.

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Other records listing Immedica, 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.

K023575CONCERT CRANIOPLASTK013755CONCERT RADIOPAQUE BONE CEMENTK003205TRANSFX ANGLED RODSK001228EXTERNAL FIXATION ANCHOR PINK001084TRANS FX ADJUSTABLE PIN TO BAR CLAMPK990848TRANSFX INTERMEDIATE EXTERNAL FIXATION SYSTEM,TRANSFX SMALL EXTERNAL FIXATION SYSTEM, TRANSFX MINI EXTERNAL FIXATION

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Related Devices (Code: LXT)

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.

K230067Para-Fix External Fixation SystemNew Paradigm BiomedicalK131636POLARUS CONNECTAcumed, LLCK132704DISTAL RADIUS VOLAR RIM PLATE STANDARD, DISTAL RADIUS VOLAR RIM PLATE NARROWBiometK112345DISTAL VOLAR RADIUS PLATING SYSTEMSMedos International SARLK090374STERILE DVR ANATOMIC PLATES VARIOUS CONFIGURATIONS) MODEL (S) 131212001,2, 5-10 2.5MM THREADED AND SMOOTH PEGS, MODEL(SDePuy Orthopaedics, Inc.K073135SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONSSynthes (Usa)

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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