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FDA 510(k)

The Progressive Orthopaedic Total Hip System

K-Number: K151424 · 2016-07-27

ApplicantThe Progressive Orthopaedic Company, LLC
Decision Date2016-07-27
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

The Progressive Orthopaedic Total Hip System is a medical device manufactured by The Progressive Orthopaedic Company, LLC. It received FDA 510(k) clearance on 2016-07-27 under approval number K151424. 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 The Progressive Orthopaedic Total Hip System?

The Progressive Orthopaedic Total Hip System is a medical device that received FDA 510(k) clearance on 2016-07-27. It is manufactured by The Progressive Orthopaedic Company, LLC. The 510(k) number is K151424.

When was The Progressive Orthopaedic Total Hip System approved by the FDA?

The Progressive Orthopaedic Total Hip System received FDA 510(k) clearance on 2016-07-27, under approval number K151424.

What company makes The Progressive Orthopaedic Total Hip System?

The Progressive Orthopaedic Total Hip System is manufactured by The Progressive Orthopaedic Company, LLC.

What is the FDA product code for The Progressive Orthopaedic Total Hip System?

The FDA product code for The Progressive Orthopaedic Total Hip System is LPH.

Related Clinical Trials

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Related PubMed Literature

PMID: 42173476 Feasibility of applying the Orthopaedic Data Evaluation Panel (ODEP) shoulder criteria for implants used in a United States-based integrated healthcare system. Journal of shoulder and elbow surgery (2026) PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026) PMID: 41966145 From Registry to Reality: Opportunities to Enhance Post-market Surveillance of High-Risk Medical Devices Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review". International journal of health policy and management (2025)

Other Devices by The Progressive Orthopaedic Company, LLC

K183344The Progressive Orthopaedic Company Total Knee System II

Related Devices (Code: LPH)

K162127Bencox M Stem Lateralized & Bencox Mirabo Cup SystemCorentec Co., Ltd. K161073Klassic HD Hip SystemTotal Joint Othopedics, Inc. K161569Trident® II Tritanium® Acetabular Shells and 6.5 mm Low Profile Hex ScrewsHowmedica Osteonics Corp. A.K.A. Stryker Orthopaedics K161184iNSitu Total Hip SystemTheken Companies, LLC K161190G7 Dual Mobility System, Active Articulation SystemBiomet, Inc. K153345Stryker Orthopaedics Hip Systems Labeling UpdateStryker Orthopaedics

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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