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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name instrument, surgical, orthopedic, pneumatic powered & accessory/attachment
510(k) Number K831756
Device Name ANSPACH 65,000
Applicant
THE ANSPACH EFFORT, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
THE ANSPACH EFFORT, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4820
Classification Product Code
HSZ  
Date Received06/01/1983
Decision Date 09/29/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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