FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ALLOPREP SYSTEM

K Number: K883065 · Decision Oct 13, 1988
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
366
Applicant Total
24
Review Days
85

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Basic Information

Device Name
ALLOPREP SYSTEM
K Number
K883065
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Osteotech, Inc.
Date Received
July 20, 1988
Decision Date
October 13, 1988
Product Code
KIT
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
KIT Media And Components, Synthetic Cell And Tissue Culture

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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
K061982 PLEXUR P
K051188 GRAFTON DBM
K051781 GRAFTCAGE TLX
K051195 GRAFTON DBM
K043209 VIAGRAF DBM PASTE
K053080 GRAFTCAGE ACX
Search all 24 clearances from Osteotech, Inc. →