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FDA 510(k)

DEPUY SIGMA PS FEMORAL COMPONENTS

K-Number: K073529 · 2008-01-24

ApplicantDePuy Orthopaedics, Inc.
Decision Date2008-01-24
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY SIGMA PS FEMORAL COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2008-01-24 under 510(k) number K073529. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY SIGMA PS FEMORAL COMPONENTS?

DEPUY SIGMA PS FEMORAL COMPONENTS is a medical device that received FDA 510(k) clearance on 2008-01-24. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K073529.

When did DEPUY SIGMA PS FEMORAL COMPONENTS receive FDA 510(k) clearance?

DEPUY SIGMA PS FEMORAL COMPONENTS received FDA 510(k) clearance on 2008-01-24, under 510(k) number K073529.

Who is the listed applicant for DEPUY SIGMA PS FEMORAL COMPONENTS?

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

What is the FDA product code for DEPUY SIGMA PS FEMORAL COMPONENTS?

The FDA product code for DEPUY SIGMA PS FEMORAL COMPONENTS is JWH.

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Other records listing DePuy Orthopaedics, Inc. as applicant

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K262130ATTUNE Revision Knee SystemK252887DePuy ATTUNE™ Knee SystemK231503CUPTIMIZE™ AdvancedK213839DePuy Corail AMT Hip ProsthesisK210167DELTA XTEND Reverse Shoulder SystemK203167DePuy Corail AMT Hip Prosthesis

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Related Devices (Code: JWH)

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.

K262057GMK ExtensionMedacta International SAK260063GSPE SpacerThe General Hospital Corporation, d/b/a MassachusettsK262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) Co., Ltd.

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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