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

MACROPORE HYDROSORB SPINE SYSTEM

K Number: K041105 · Decision Jul 28, 2004
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
17
Review Days
89

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Basic Information

Device Name
MACROPORE HYDROSORB SPINE SYSTEM
K Number
K041105
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Macropore Biosurgery, Inc.
Date Received
April 30, 2004
Decision Date
July 28, 2004
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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Other Clearances by Macropore Biosurgery, Inc.

K Number Device Name
K042261 MACROPORE PURICEL LIPOPLASTY 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
K011715 MACROPORE IB RESORBABLE PLUG
Search all 17 clearances from Macropore Biosurgery, Inc. →