FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OsteoRemedies Hip Spacer System

K Number: K253675 · Decision Dec 23, 2025
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
11
Review Days
32

Basic Information

Device Name
OsteoRemedies Hip Spacer System
K Number
K253675
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteoremedies, LLC
Date Received
November 21, 2025
Decision Date
December 23, 2025
Product Code
KWL
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KWL Prosthesis, Hip, Hemi-, Femoral, Metal

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Other Clearances by Osteoremedies, LLC

K Number Device Name
K250760 SPECTRUM GV Bone Cement
K242377 REMEDY Stemmed Knee Spacer System with All-Poly Tibial Component
K231556 SPECTRUM® GV Bone Cement
K223650 REMEDY Stemmed Knee Spacer
K192995 OsteoRemedies Hip Spacer System
K191981 REMEDY Acetabular Cup
K183017 Remedy Femoral Component 84mm, Remedy Stemmed Knee Spacer
K172906 REMEDY PLUS Hip Spacer, UNITE PLUS Bone Cement
K173967 Remedy Acetabular Cup
K152267 Remedy® Shoulder Spacer
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