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

ACCELL EVO3C

K Number: K091193 · Decision Aug 10, 2009
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
30
Applicant Total
10
Review Days
109

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Basic Information

Device Name
ACCELL EVO3C
K Number
K091193
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
April 23, 2009
Decision Date
August 10, 2009
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MBP), ordered by most recent decision date.

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Other Clearances by Isotis Orthobiologics, Inc.

K Number Device Name
K081817 ACCELL TBM-R
K070751 ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY
K050642 ORTHOBLAST II PUTTY AND PASTE
K052098 CONNEXUS, .5CC, MODEL 023000-005
K043573 DYNAGRAFT II DENTAL
K050690 CONNEXUS
K040419 DYNAGRAFT II
K042706 OSSATURA DENTAL
K041991 ASPIREX - BONE MARROW ASPIRATE KIT