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

THERIRIDGE BLOCK, BONE GRAFT SUBSTITUTE

K Number: K023998 · Decision Mar 26, 2003
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
3
Review Days
113

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THERIRIDGE BLOCK, BONE GRAFT SUBSTITUTE
K Number
K023998
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Therics, Inc.
Date Received
December 3, 2002
Decision Date
March 26, 2003
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.

View all

Other Clearances by Therics, Inc.

K Number Device Name
K040134 THERILINK BONE VOID FILLER
K031040 THERIFIL BONE FILLER