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

ACCELL TBM-R

K Number: K081817 · Decision Sep 24, 2008
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
30
Applicant Total
10
Review Days
90

Basic Information

Device Name
ACCELL TBM-R
K Number
K081817
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ISOTIS ORTHOBIOLOGICS, INC
Date Received
June 26, 2008
Decision Date
September 24, 2008
Product Code
MBP
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
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

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