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FDA 510(k)

DePuy Corail AMT Hip Prosthesis

K-Number: K203167 · 2020-11-19

ApplicantDePuy Orthopaedics, Inc.
Decision Date2020-11-19
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy Corail AMT Hip Prosthesis 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 2020-11-19 under 510(k) number K203167. 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 DePuy Corail AMT Hip Prosthesis?

DePuy Corail AMT Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2020-11-19. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K203167.

When did DePuy Corail AMT Hip Prosthesis receive FDA 510(k) clearance?

DePuy Corail AMT Hip Prosthesis received FDA 510(k) clearance on 2020-11-19, under 510(k) number K203167.

Who is the listed applicant for DePuy Corail AMT Hip Prosthesis?

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 Corail AMT Hip Prosthesis?

The FDA product code for DePuy Corail AMT Hip Prosthesis is LZO.

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Other records listing DePuy Orthopaedics, 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.

PMA P070026Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncementedK252887DePuy ATTUNE™ Knee SystemK231503CUPTIMIZE™ AdvancedK213839DePuy Corail AMT Hip ProsthesisK210167DELTA XTEND Reverse Shoulder SystemK202472ACTIS Duofix Hip Prosthesis

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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.

K261009MobileLink 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 GmbHK252401implaFit® short stemsImplantcast GmbHK253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)Maxx Orthopedics, 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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