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FDA 510(k)

SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM

K-Number: K001320 · 2000-07-07

ApplicantSulzer Orthopedics, Inc.
Decision Date2000-07-07
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM is the device name listed in this FDA 510(k) record. The listed applicant is Sulzer Orthopedics, Inc.. It received FDA 510(k) clearance on 2000-07-07 under 510(k) number K001320. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM?

SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM is a medical device that received FDA 510(k) clearance on 2000-07-07. The listed applicant is Sulzer Orthopedics, Inc.. The 510(k) number is K001320.

When did SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM receive FDA 510(k) clearance?

SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM received FDA 510(k) clearance on 2000-07-07, under 510(k) number K001320.

Who is the listed applicant for SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM?

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

What is the FDA product code for SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM?

The FDA product code for SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM is LPH.

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Other records listing Sulzer Orthopedics, 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.

K022985ASCENDENT ACETABULAR SYSTEMK021578NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATEK020713MS-30 LATERAL FEMORAL STEMK013935ALLOFIT ACETABULAR SYSTEM 32MM ALPHA DURASUL INSERTSK013031MOST OPTIONS SYSTEMK012739CONVERGE ACETABULAR SYSTEM

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Related Devices (Code: LPH)

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.

K261453G7® Acetabular SystemZimmer BiometK253630Mpact 3D Metal FoamMedacta International S.A.K254043TRIVANCE™ Hip StemGlobus Medical, Inc.K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi CoatingNextstep Arthopedix, LLCK251270Taperloc® Complete Hip StemBiomet, 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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