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

PLEXUR P

K Number: K061982 · Decision Feb 7, 2007
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
30
Applicant Total
24
Review Days
209

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Basic Information

Device Name
PLEXUR P
K Number
K061982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteotech, Inc.
Date Received
July 13, 2006
Decision Date
February 7, 2007
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 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
K051188 GRAFTON DBM
K051781 GRAFTCAGE TLX
K051195 GRAFTON DBM
K043209 VIAGRAF DBM PASTE
K053080 GRAFTCAGE ACX
K042707 GRAFTON PLUS DBM PASTE
Search all 24 clearances from Osteotech, Inc. →