FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

WILLIAMS VERTEBRAL SPREADER

K Number: K872858 · Decision Oct 15, 1987
Classifications
1
FEI Numbers
162
Registration Numbers
162
Same Product Code
4
Applicant Total
21
Review Days
86

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Basic Information

Device Name
WILLIAMS VERTEBRAL SPREADER
K Number
K872858
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Ace Medical Co.
Date Received
July 21, 1987
Decision Date
October 15, 1987
Product Code
HXP
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
HXP Instrument, Bending Or Contouring

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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
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