ALTOMEC ARTHROSCOPE


Device Classification Name

arthroscope

510(k) Number K112548
Device Name ALTOMEC ARTHROSCOPE
Applicant
ALTOMEC ENDOSCOPY INC
7305 hancock village dr.
suite 109
chesterfield, 
VA 
23832

Applicant Contact darren reeves
Correspondent
ALTOMEC ENDOSCOPY INC
7305 hancock village dr.
suite 109
chesterfield, 
VA 
23832

Correspodent Contact darren reeves
Regulation Number 888.1100
Classification Product Code
HRX  
Date Received 09/01/2011
Decision Date 08/15/2012
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

General & Plastic Surgery

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No