FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

GENEX BONE GRAFT SUBSTITUTE

K Number: K040600 · Decision May 7, 2004
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
27
Review Days
60

Basic Information

Device Name
GENEX BONE GRAFT SUBSTITUTE
K Number
K040600
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biocomposites, Ltd.
Date Received
March 8, 2004
Decision Date
May 7, 2004
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

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

View all

Other Clearances by Biocomposites, Ltd.

K Number Device Name
K251680 Biosteon® Screw
K242865 Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer
K250521 NanoBone® SBX Putty ; NanoBone® QD
K212721 Genex Bone Graft Substitute
K141830 STIMULAN KIT, STIMULAN RAPID CURE
K082381 GENEX
K082383 FORTOSS VITAL
K073341 GENEX PUTTY
K081428 MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR
K072127 DOMINATOR
Search all 27 clearances from Biocomposites, Ltd. →