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FDA 510(k)

MRP-TITAN

K-Number: K992403 · 2000-01-21

ApplicantRotec Medizintechnik GmbH
Decision Date2000-01-21
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MRP-TITAN is the device name listed in this FDA 510(k) record. The listed applicant is Rotec Medizintechnik GmbH. It received FDA 510(k) clearance on 2000-01-21 under 510(k) number K992403. 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 MRP-TITAN?

MRP-TITAN is a medical device that received FDA 510(k) clearance on 2000-01-21. The listed applicant is Rotec Medizintechnik GmbH. The 510(k) number is K992403.

When did MRP-TITAN receive FDA 510(k) clearance?

MRP-TITAN received FDA 510(k) clearance on 2000-01-21, under 510(k) number K992403.

Who is the listed applicant for MRP-TITAN?

The FDA 510(k) record lists Rotec Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRP-TITAN?

The FDA product code for MRP-TITAN is LZO.

Related Clinical Trials

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.

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Other records listing Rotec Medizintechnik GmbH 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.

K992359MRS-TITAN

Related Devices (Code: LZO)

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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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