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

SPREADER

K Number: K781445 · Decision Sep 27, 1979
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
45
Review Days
400

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Basic Information

Device Name
SPREADER
K Number
K781445
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Orthopedic Equipment Co., Inc.
Date Received
August 23, 1978
Decision Date
September 27, 1979
Product Code
GAD
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
GAD Retractor

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GAD), 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
K790247 TOURNIQUET TEST GAGE
K790209 FILTER SYSTEM, ALTNER DISPOSABLE
K781450 DRIVERS
K781444 OUTRIGGER DISTRACTION UNIT
K781451 FLAT WRENCH
K781447 THREADED ROD CLAMP
K781449 HARRINGTON SPINAL ELEVATOR
Search all 45 clearances from Orthopedic Equipment Co., Inc. →