FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇷 Türkiye

OGM 1 Polymethylmethacrylate (PMMA) bone cement, OGM 1A Polymethylmethacrylate (PMMA) bone cement

K Number: K211869 · Decision May 19, 2022
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
71
Applicant Total
1
Review Days
337

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Basic Information

Device Name
OGM 1 Polymethylmethacrylate (PMMA) bone cement, OGM 1A Polymethylmethacrylate (PMMA) bone cement
K Number
K211869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ormed Grup Medikal Turizm Saglik Hizmetleri Sanayi VE
Date Received
June 16, 2021
Decision Date
May 19, 2022
Product Code
LOD
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
LOD Bone Cement

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