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

CEMENT EXTRACTION INSTRUMENT SET

K Number: K780135 · Decision Jan 31, 1978
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
10
Applicant Total
45
Review Days
7

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Basic Information

Device Name
CEMENT EXTRACTION INSTRUMENT SET
K Number
K780135
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Orthopedic Equipment Co., Inc.
Date Received
January 24, 1978
Decision Date
January 31, 1978
Product Code
KDG
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDG Chisel (Osteotome)

Similar 510(k) Clearances

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

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Other Clearances by Orthopedic Equipment Co., Inc.

K Number Device Name
K834035 UNIVERSAL SELF-ALIGNING ACETABULAR COM
K841189 OEC/REZAIAN SPINAL FIXATOR
K800530 SCHLEIN TRI-SURFACE ANKLE
K781445 SPREADER
K790247 TOURNIQUET TEST GAGE
K790209 FILTER SYSTEM, ALTNER DISPOSABLE
K781450 DRIVERS
K781444 OUTRIGGER DISTRACTION UNIT
K781451 FLAT WRENCH
K781447 THREADED ROD CLAMP
Search all 45 clearances from Orthopedic Equipment Co., Inc. →