FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

MACROPORE IB RESORBABLE PLUG

K Number: K011715 · Decision Aug 27, 2001
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
17
Review Days
84

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Basic Information

Device Name
MACROPORE IB RESORBABLE PLUG
K Number
K011715
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Unknown
Statement or Summary
Summary
Applicant
Macropore Biosurgery, Inc.
Date Received
June 4, 2001
Decision Date
August 27, 2001
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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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. →