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FDA 510(k)

TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS

K-Number: K933108 · 1994-09-12

ApplicantLandos, Inc.
Decision Date1994-09-12
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Landos, Inc.. It received FDA 510(k) clearance on 1994-09-12 under 510(k) number K933108. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS?

TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1994-09-12. The listed applicant is Landos, Inc.. The 510(k) number is K933108.

When did TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS receive FDA 510(k) clearance?

TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS received FDA 510(k) clearance on 1994-09-12, under 510(k) number K933108.

Who is the listed applicant for TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS?

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

What is the FDA product code for TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS?

The FDA product code for TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS is LZO.

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Related Devices (Code: LZO)

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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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