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

MODIFICATION TO SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM

K Number: K063497 · Decision Dec 19, 2006
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
6
Review Days
29

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Basic Information

Device Name
MODIFICATION TO SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
K Number
K063497
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Scandius Biomedical, Inc.
Date Received
November 20, 2006
Decision Date
December 19, 2006
Product Code
MAI
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
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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Other Clearances by Scandius Biomedical, Inc.

K Number Device Name
K063499 MODIFICATION TO SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
K060522 SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
K052810 SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
K041961 SCANDIUS ABSORBABLE ACL RECONSTRUCTION SYSTEM
K041749 SCANDIUS ACL RECONSTRUCTION SYSTEM