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

CAP BONE SUBSTITUTE MATERIAL

K Number: K032307 · Decision Oct 24, 2003
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
43
Applicant Total
18
Review Days
91

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Basic Information

Device Name
CAP BONE SUBSTITUTE MATERIAL
K Number
K032307
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5300
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Etex Corp.
Date Received
July 25, 2003
Decision Date
October 24, 2003
Product Code
GXP
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GXP Methyl Methacrylate For Cranioplasty

Similar 510(k) Clearances

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

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Other Clearances by Etex Corp.

K Number Device Name
K100883 CARRIGEN
K101557 GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN
K093447 CARRIGEN
K091729 ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
K091607 ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
K090855 EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
K090310 EQUIVABONE
K090242 GAMMA-BSM, BETA-BSM
K080329 CAP PLUS, EQUIVABONE, CAP/DBM
K063050 CAP PLUS
Search all 18 clearances from Etex Corp. →