FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MACROPORENS CRANILOC

K Number: K002334 · Decision May 2, 2001
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
28
Applicant Total
17
Review Days
274

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Basic Information

Device Name
MACROPORENS CRANILOC
K Number
K002334
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5250
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Macropore Biosurgery, Inc.
Date Received
August 1, 2000
Decision Date
May 2, 2001
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

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Other Clearances by Macropore Biosurgery, Inc.

K Number Device Name
K042261 MACROPORE PURICEL LIPOPLASTY SYSTEM
K041105 MACROPORE HYDROSORB SPINE SYSTEM
K031955 MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET
K031785 MACROPORE CARDIO-WRAP (TS)
K024169 MACROPORE OS RECONSTRUCTION
K023643 MACROPORE SURGICAL BARRIER FILM
K021164 MACROPORE OS TRAUMA
K012025 MACROPORE SURGIWRAP (TS)
K012769 MACROPORE ENT RECONSTRUCTION FILM
K012413 MACROPORE FX, PS, NS, LP
Search all 17 clearances from Macropore Biosurgery, Inc. →