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

WEBER PERMALOCK

K Number: K896669 · Decision Feb 6, 1990
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
16
Review Days
71

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Basic Information

Device Name
WEBER PERMALOCK
K Number
K896669
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Allo Pro Corp.
Date Received
November 27, 1989
Decision Date
February 6, 1990
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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Other Clearances by Allo Pro Corp.

K Number Device Name
K901581 GSB ELBOW
K900425 SURGICAL COTTON GLOVES
K900392 CENTERING PLUG
K892644 BIOLOX CERAMIC BALL
K885049 RS-CUP ACETABULAR PROSTHESIS
K864999 KENNEDY STEM
K871453 ZWEYMUELLER-SL HIP PROSTHESIS STEM
K851213 ZWEYMULLER CUP
K841391 WEBER-STUHMER HIP PROSTHESIS STEM
K830948 WEBER/STIIHMER FEMORAL HEAD PROSTHESIS
Search all 16 clearances from Allo Pro Corp. →