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

J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030

K Number: K101902 · Decision Feb 8, 2011
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
53
Review Days
215

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
J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030
K Number
K101902
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jeil Medical Corporation
Date Received
July 8, 2010
Decision Date
February 8, 2011
Product Code
DZL
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
DZL Screw, Fixation, Intraosseous

Similar 510(k) Clearances

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

View all

Other Clearances by Jeil Medical Corporation

K Number Device Name
K252246 Leforte MMF System
K252826 ARIX Femur Nail System
K251431 FIX-C PEEK ACIF SA System
K243973 FIX-L PEEK PLIF and T-PLIF System
K242751 ARIX Pectus Bar System
K242247 ARIX Femur Nail System
K243915 FIX-C 3D Ti ACIF System
K243004 Xpine Spinal Fixation System
K231251 FlexWing Anterior Cervical Plate System
K233912 ARIX Cannulated Screw System
Search all 53 clearances from Jeil Medical Corporation →