FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

OsteoSinter® EVANS and COTTON wedges and related accessories

K Number: K240461 · Decision Dec 6, 2024
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
17
Applicant Total
1
Review Days
294

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Basic Information

Device Name
OsteoSinter® EVANS and COTTON wedges and related accessories
K Number
K240461
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ames Medical Prosthetic Solutions, S.A.U.
Date Received
February 16, 2024
Decision Date
December 6, 2024
Product Code
PLF
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
PLF Bone Wedge

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