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

OSSIFORM

K Number: K020720 · Decision May 7, 2002
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
7
Review Days
63

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Basic Information

Device Name
OSSIFORM
K Number
K020720
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Unicare Biomedical, Inc.
Date Received
March 5, 2002
Decision Date
May 7, 2002
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

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Other Clearances by Unicare Biomedical, Inc.

K Number Device Name
K151344 Cytoflex Tefguard Ti-Enforced Membrane
K092567 MODIFICATION TO UNIGRAFT
K090083 CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
K080532 BENACEL, MODELS C-001, C-002 AND C-005
K021511 CYTOFLEX MESH
K012144 CYTOFLEX