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

MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079

K Number: K101835 · Decision Dec 3, 2010
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
6
Applicant Total
19
Review Days
155

Basic Information

Device Name
MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
K Number
K101835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5360
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
POREX SURGICAL, INC.
Date Received
July 1, 2010
Decision Date
December 3, 2010
Product Code
HBW
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
HBW Fastener, Plate, Cranioplasty

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Other Clearances by POREX SURGICAL, INC.

K Number Device Name
K102184 MEDPOR CONTAIN CAN IMPLANT
K091807 MEDPOR FIXATION SYSTEM
K091120 MEDPOR CONTAIN IMPLANT
K083621 MEDPOR CUSTOMIZED SURGICAL IMPLANT
K071335 MEDPOR ATTRACTOR IMPLANT
K052297 POREX ELECTROSURGERY NEEDLE
K040851 MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM
K040364 MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH
K021357 MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT
K012350 MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL
Search all 19 clearances from POREX SURGICAL, INC. →