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

POLYETHYLENE MEDULLARY PLUG - STIIHMER/

K Number: K830949 · Decision Apr 12, 1983
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
36
Applicant Total
16
Review Days
19

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Basic Information

Device Name
POLYETHYLENE MEDULLARY PLUG - STIIHMER/
K Number
K830949
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Allo Pro Corp.
Date Received
March 24, 1983
Decision Date
April 12, 1983
Product Code
LZN
Advisory Committee
General, Plastic Surgery
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
LZN Cement Obturator

Similar 510(k) Clearances

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Other Clearances by Allo Pro Corp.

K Number Device Name
K901581 GSB ELBOW
K900425 SURGICAL COTTON GLOVES
K900392 CENTERING PLUG
K896669 WEBER PERMALOCK
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
Search all 16 clearances from Allo Pro Corp. →