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FDA 510(k)

MODULAR CATHCART FRACTURE SYSTEM

K-Number: K903084 · 1990-10-03

ApplicantDepuy, Inc.
Decision Date1990-10-03
Product CodeLZY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODULAR CATHCART FRACTURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1990-10-03 under 510(k) number K903084. The device is classified under product code LZY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR CATHCART FRACTURE SYSTEM?

MODULAR CATHCART FRACTURE SYSTEM is a medical device that received FDA 510(k) clearance on 1990-10-03. The listed applicant is Depuy, Inc.. The 510(k) number is K903084.

When did MODULAR CATHCART FRACTURE SYSTEM receive FDA 510(k) clearance?

MODULAR CATHCART FRACTURE SYSTEM received FDA 510(k) clearance on 1990-10-03, under 510(k) number K903084.

Who is the listed applicant for MODULAR CATHCART FRACTURE SYSTEM?

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

What is the FDA product code for MODULAR CATHCART FRACTURE SYSTEM?

The FDA product code for MODULAR CATHCART FRACTURE SYSTEM is LZY.

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Other records listing Depuy, 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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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Related Devices (Code: LZY)

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.

K231448TANDEM Hip SystemSmith & Nephew, Inc.K111145ENDO HEADMedacta InternationalK974442PRE-POWDERED NITRILE EXAMINATION GLOVESP.T. Latexindo TobaperkasaK915528BHR BIPOLAR FEMORAL HEAD COMPONENTImplantology Corp.K915548IONGUARD TITANIUM MODULAR HEADSBiomet, Inc.K896580UNI-POLAR HEADRichards Medical Co., Inc.

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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