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

ACE-DUPONT COMPOSITE RINGS

K Number: K955388 · Decision Jan 31, 1996
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
56
Applicant Total
21
Review Days
68

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Basic Information

Device Name
ACE-DUPONT COMPOSITE RINGS
K Number
K955388
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ace Medical Co.
Date Received
November 24, 1995
Decision Date
January 31, 1996
Product Code
LXT
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
LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Similar 510(k) Clearances

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

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Other Clearances by Ace Medical Co.

K Number Device Name
K972183 DEPUY ACE A.I.M. TITANIUM TIBIAL NAIL
K955472 ACE HUMERUS & RADIUS PLATES
K954485 6.5MM SOLID CANCELLOUS BONE SCREW
K954069 ACE CERVICAL TRACTION HALOZS, TONGS & PINS
K950618 ACE SUPRACONDYLAR PLATE
K933968 ACE PELVIC STABILIZER
K931652 ACE 6.5 MM BONE SCREW
K930592 ACE UNIVERSAL RECONSTRUCTION PLATE
K912598 ACE CORTICAL BONE SCREW
K914858 ACE OPEN-BACK HALO RING
Search all 21 clearances from Ace Medical Co. →