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

OSSDSIGN Cranioplug

K Number: K181539 · Decision Oct 12, 2018
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
28
Applicant Total
6
Review Days
123

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Basic Information

Device Name
OSSDSIGN Cranioplug
K Number
K181539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5250
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ossdsign AB
Date Received
June 11, 2018
Decision Date
October 12, 2018
Product Code
GXR
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXR Cover, Burr Hole

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GXR), ordered by most recent decision date.

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Other Clearances by Ossdsign AB

K Number Device Name
K232315 Catalyst Bone Void Filler
K212414 OSSDSIGN Cranial PSI
K190523 Cranial PSI Accessory – Anatomical Model Original, Cranial PSI Accessory – Anatomical Model Modified, Cranial PSI Accessory – Plastic Drawing Guide, Cranial PSI Accessory – Cranial Implant Trial
K161090 Cranial PSI
K140309 CRANIOPLUG