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

MEDPOR ATTRACTOR IMPLANT

K Number: K071335 · Decision Aug 8, 2007
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
38
Applicant Total
19
Review Days
89

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Basic Information

Device Name
MEDPOR ATTRACTOR IMPLANT
K Number
K071335
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.3320
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Porex Surgical, Inc.
Date Received
May 11, 2007
Decision Date
August 8, 2007
Product Code
HPZ
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HPZ Implant, Eye Sphere

Similar 510(k) Clearances

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Other Clearances by Porex Surgical, Inc.

K Number Device Name
K102184 MEDPOR CONTAIN CAN IMPLANT
K101835 MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
K091807 MEDPOR FIXATION SYSTEM
K091120 MEDPOR CONTAIN IMPLANT
K083621 MEDPOR CUSTOMIZED SURGICAL 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. →