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FDA 510(k)

TITAN DYSPLASIC TOTAL HIP PROSTHESIS

K-Number: K932935 · 1994-06-15

ApplicantLandos, Inc.
Decision Date1994-06-15
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITAN DYSPLASIC 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 1994-06-15 under 510(k) number K932935. 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 DYSPLASIC TOTAL HIP PROSTHESIS?

TITAN DYSPLASIC TOTAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1994-06-15. The listed applicant is Landos, Inc.. The 510(k) number is K932935.

When did TITAN DYSPLASIC TOTAL HIP PROSTHESIS receive FDA 510(k) clearance?

TITAN DYSPLASIC TOTAL HIP PROSTHESIS received FDA 510(k) clearance on 1994-06-15, under 510(k) number K932935.

Who is the listed applicant for TITAN DYSPLASIC 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 DYSPLASIC TOTAL HIP PROSTHESIS?

The FDA product code for TITAN DYSPLASIC TOTAL HIP PROSTHESIS is LZO.

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Other records listing Landos, Inc. as applicant

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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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