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

ENTRAX TRACTION UNIT

K Number: K780763 · Decision May 16, 1978
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
0
Applicant Total
45
Review Days
8

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Basic Information

Device Name
ENTRAX TRACTION UNIT
K Number
K780763
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.5890
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Orthopedic Equipment Co., Inc.
Date Received
May 8, 1978
Decision Date
May 16, 1978
Product Code
HSR
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
HSR Unit, Traction, Hip, Non-Powered, Non-Penetrating

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. →