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

HIP FIXATION SYSTEM

K Number: K950866 · Decision May 30, 1995
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
41
Review Days
92

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
HIP FIXATION SYSTEM
K Number
K950866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medtec, Inc.
Date Received
February 27, 1995
Decision Date
May 30, 1995
Product Code
IYE
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IYE Accelerator, Linear, Medical

Similar 510(k) Clearances

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

View all

Other Clearances by Medtec, Inc.

K Number Device Name
K132908 TRUPOINT ARCH, NASION CUSHION, BITE CUP, TRUPOINT ARCH STORAGE PLATE, TRUPOINT ARCH BASE LOCK REPLACEMENT KIT
K111340 HEAD AND NECK IMMOBILIZATION SYSTEM, BODY IMMOBILIZATION SYSTEM
K093738 MRI PATIENT POSITIONING DEVICES
K974703 CARBON FIBER BREAST BOARD
K974700 MATRIX MT-MX3
K973842 CARBON FIBER CONFORMAL COUCH TOP
K962622 INTRA-ORAL THERMOPLASTIC SHIELD
K955236 GREEN TEC-2100
K954705 ACRYSTEEL BLOCKING TRAY
K954456 THERMOPLASTIC SHIELD
Search all 41 clearances from Medtec, Inc. →