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

BSM BONE SUBSTITUTE MATERIAL KIT

K Number: K962548 · Decision Aug 5, 1997
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
18
Review Days
403

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Basic Information

Device Name
BSM BONE SUBSTITUTE MATERIAL KIT
K Number
K962548
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Etex Corp.
Date Received
June 28, 1996
Decision Date
August 5, 1997
Product Code
LYC
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
LYC Bone Grafting Material, Synthetic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYC), 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. →