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

ACE EXTERNAL BONE CLAMP PART #S11

K Number: K791466 · Decision Aug 16, 1979
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
84
Applicant Total
14
Review Days
15

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
ACE EXTERNAL BONE CLAMP PART #S11
K Number
K791466
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Ace Orthopedic Manufacturing Co.
Date Received
August 1, 1979
Decision Date
August 16, 1979
Product Code
JEC
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
JEC Component, Traction, Invasive

Similar 510(k) Clearances

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

View all

Other Clearances by Ace Orthopedic Manufacturing Co.

K Number Device Name
K934643 ACE HUMERAL NAIL
K934962 AIM SUPRACONDYLAR NAIL
K936045 ACE UNILATERAL FIXATOR II
K926047 ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW
K920738 ACE 100 DEGREES TUBULAR PLATE
K813554 ACE/KYLE CAPTURED HIP SCREW
K810193 TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG
K801594 ACE FISCHER EXTERNAL FIXATION DEVICE
K781839 BONE CLAMP, ACE EXTERNAL
K781840 EXTERNAL ARTICULATION
Search all 14 clearances from Ace Orthopedic Manufacturing Co. →