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

PLEXUR-P

K Number: K080511 · Decision Apr 21, 2008
Classifications
1
FEI Numbers
234
Registration Numbers
234
Same Product Code
483
Applicant Total
23
Review Days
56

Basic Information

Device Name
PLEXUR-P
K Number
K080511
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
February 25, 2008
Decision Date
April 21, 2008
Product Code
MQV
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
MQV Filler, Bone Void, Calcium Compound

Similar 510(k) Clearances

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Other Clearances by OSTEOTECH, INC.

K Number Device Name
K081227 PLEXUR M
K073405 PLEXUR M
K061982 PLEXUR P
K051188 GRAFTON DBM
K051781 GRAFTCAGE TLX
K051195 GRAFTON DBM
K043209 VIAGRAF DBM PASTE
K053080 GRAFTCAGE ACX
K042707 GRAFTON PLUS DBM PASTE
K043048 GRAFTON PLUS DBM PASTE
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