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

ACE CANCELLOUS BONE SCREW

K Number: K872859 · Decision Aug 17, 1987
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
21
Review Days
27

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Basic Information

Device Name
ACE CANCELLOUS BONE SCREW
K Number
K872859
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Ace Medical Co.
Date Received
July 21, 1987
Decision Date
August 17, 1987
Product Code
HWC
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
HWC Screw, Fixation, Bone

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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
K955388 ACE-DUPONT COMPOSITE RINGS
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
Search all 21 clearances from Ace Medical Co. →