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FDA 510(k)

REMEDY POLY+PLUS SNAP FIT Acetabular Cup

K-Number: K262290 · 2026-07-24

ApplicantOsteoremedies, LLC
Decision Date2026-07-24
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REMEDY POLY+PLUS SNAP FIT Acetabular Cup is the device name listed in this FDA 510(k) record. The listed applicant is Osteoremedies, LLC. It received FDA 510(k) clearance on 2026-07-24 under 510(k) number K262290. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMEDY POLY+PLUS SNAP FIT Acetabular Cup?

REMEDY POLY+PLUS SNAP FIT Acetabular Cup is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is Osteoremedies, LLC. The 510(k) number is K262290.

When did REMEDY POLY+PLUS SNAP FIT Acetabular Cup receive FDA 510(k) clearance?

REMEDY POLY+PLUS SNAP FIT Acetabular Cup received FDA 510(k) clearance on 2026-07-24, under 510(k) number K262290.

Who is the listed applicant for REMEDY POLY+PLUS SNAP FIT Acetabular Cup?

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

What is the FDA product code for REMEDY POLY+PLUS SNAP FIT Acetabular Cup?

The FDA product code for REMEDY POLY+PLUS SNAP FIT Acetabular Cup is KWL.

Other records listing Osteoremedies, LLC 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.

K253675OsteoRemedies Hip Spacer SystemK250760SPECTRUM GV Bone CementK242377REMEDY Stemmed Knee Spacer System with All-Poly Tibial ComponentK231556SPECTRUM® GV Bone CementK223650REMEDY Stemmed Knee SpacerK192995OsteoRemedies Hip Spacer System

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Related Devices (Code: KWL)

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.

K260536Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone CementDepuy Ireland UCK253675OsteoRemedies Hip Spacer SystemOsteoremedies, LLCK252326InterSpace GV Hip SpacerTecres S.P.A.K242865Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder SpacerBiocomposites, Ltd.K234028COPAL® exchange G hip spacer; COPAL® G+VHeraeus Medical GmbHK222632UHR Bipolar Implants, Restoration GAP II ImplantsHowmedica Osteonics Corp., Dba Stryker 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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