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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K760001
Device Name ARCH SUPPORT (ARCH AID)
Applicant
ZIMMER, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
ZIMMER, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Date Received05/26/1976
Decision Date 07/26/1976
Decision Substantially Equivalent (SESE)
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
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