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

COMPRESSION CERCLAGE GUNDOLF CCG-GF

K Number: K973098 · Decision Oct 27, 1997
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
38
Review Days
69

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
COMPRESSION CERCLAGE GUNDOLF CCG-GF
K Number
K973098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Plus Orthopedics
Date Received
August 19, 1997
Decision Date
October 27, 1997
Product Code
JDQ
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
JDQ Cerclage, Fixation

Similar 510(k) Clearances

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

View all

Other Clearances by Plus Orthopedics

K Number Device Name
K032126 PROMOS SHOULDER
K033763 MODIFICATION TO SLIM GLIDING NAIL SYSTEM
K032709 MODULAR PLUS HIP STEM
K032548 IP-XS COMPRESSION NAIL SYSTEM
K032215 VKS/TC-PLUS REVISION KNEE
K032052 UC-PLUS SOLUTION UNICONDYLAR KNEE
K031165 PLUS ORTHOPEDICS CEMENTED HIP STEM
K030971 MODIFICATION TO MODULAR PLUS REVISION STEM
K024134 UNI HIP STEM
K023667 RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE
Search all 38 clearances from Plus Orthopedics →