FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds

K Number: K240856 · Decision Nov 20, 2024
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
18
Applicant Total
6
Review Days
237

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Basic Information

Device Name
Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds
K Number
K240856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osartis GmbH
Date Received
March 28, 2024
Decision Date
November 20, 2024
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
K202458 BonOs Inject, Pedicle screw kits, Cement pusher
K210120 BonOs HV, BonOs MV, BonOs LV
K210125 BonOs HV Genta, BonOs MV Genta, BonOs LV Genta
K192394 Hi-Fatigue Bone Cement
K192379 Hi-Fatigue G Bone Cement