FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

SpaceFix Shoulder Spacer

K Number: K252443 · Decision Sep 15, 2025
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
18
Applicant Total
12
Review Days
42

Basic Information

Device Name
SpaceFix Shoulder Spacer
K Number
K252443
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
G21, S.R.L.
Date Received
August 4, 2025
Decision Date
September 15, 2025
Product Code
MBB
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
MBB Bone Cement, Antibiotic

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K Number Device Name
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K193061 G3 40 Radiopaque Bone Cement
K192041 G21 SpaceFlex Hip
K190216 SpaceFlex Knee
K181282 G3A 40 Bone Cement
K173494 OrthoSteady G Bone Cement
K152557 Winch Kyphoplasty(15 and 20 mm) 11 Gauge Balloon Catheters
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