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

ACE 6.5 MM BONE SCREW

K Number: K931652 · Decision Apr 28, 1994
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
21
Review Days
388

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 6.5 MM BONE SCREW
K Number
K931652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Ace Medical Co.
Date Received
April 5, 1993
Decision Date
April 28, 1994
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

Similar 510(k) Clearances

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

View all

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
K930592 ACE UNIVERSAL RECONSTRUCTION PLATE
K912598 ACE CORTICAL BONE SCREW
K914858 ACE OPEN-BACK HALO RING
Search all 21 clearances from Ace Medical Co. →