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

GRAFTON PLUS DBM PASTE

K Number: K042707 · Decision Nov 30, 2005
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
14
Applicant Total
24
Review Days
426

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Basic Information

Device Name
GRAFTON PLUS DBM PASTE
K Number
K042707
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteotech, Inc.
Date Received
September 30, 2004
Decision Date
November 30, 2005
Product Code
NUN
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NUN Bone Grafting Material, Human Source

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Other Clearances by Osteotech, Inc.

K Number Device Name
K082615 GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES
K081227 PLEXUR M
K080511 PLEXUR-P
K073405 PLEXUR M
K061982 PLEXUR P
K051188 GRAFTON DBM
K051781 GRAFTCAGE TLX
K051195 GRAFTON DBM
K043209 VIAGRAF DBM PASTE
K053080 GRAFTCAGE ACX
Search all 24 clearances from Osteotech, Inc. →