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

Oyster ACIF Cage

K Number: K182608 · Decision Jun 13, 2019
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
12
Review Days
265

Basic Information

Device Name
Oyster ACIF Cage
K Number
K182608
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Silony Medical GmbH
Date Received
September 21, 2018
Decision Date
June 13, 2019
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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