Cleared Traditional

C.S.M. HIP

K862752 · Protek, Inc. · Orthopedic

Aug 1986

Decision

16d

Days

—

Risk

About This 510(k) Submission

K862752 is an FDA 510(k) clearance for the C.S.M. HIP, submitted by Protek, Inc. (Indianapolis, US). The FDA issued a Cleared decision on August 7, 1986, 16 days after receiving the submission on July 22, 1986. This device falls under the Orthopedic review panel.

Submission Details

510(k) Number	K862752 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 22, 1986
Decision Date	August 07, 1986
Days to Decision	16 days
Submission Type	Traditional
Review Panel	Orthopedic (OR)
Summary	—