Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

C.S.M. HIP

K-Number: K862752 · 1986-08-07

ApplicantProtek, Inc.
Decision Date1986-08-07
Product Code
DecisionSubstantially Equivalent

Device Summary

C.S.M. HIP is the device name listed in this FDA 510(k) record. The listed applicant is Protek, Inc.. It received FDA 510(k) clearance on 1986-08-07 under 510(k) number K862752. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.S.M. HIP?

C.S.M. HIP is a medical device that received FDA 510(k) clearance on 1986-08-07. The listed applicant is Protek, Inc.. The 510(k) number is K862752.

When did C.S.M. HIP receive FDA 510(k) clearance?

C.S.M. HIP received FDA 510(k) clearance on 1986-08-07, under 510(k) number K862752.

Who is the listed applicant for C.S.M. HIP?

The FDA 510(k) record lists Protek, Inc. as the applicant. This does not by itself establish the device manufacturer.

Other records listing Protek, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K893785ARC-2F ACETABULAR CUPK893959P.S.A. FEMORAL HIP PROSTHESISK892059FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SURK883794RESUBMITTED CLW ACETABULAR CUP W/SULMESHK884952VARIOUS FEMORAL HIP PROSTHESES W/SELF LOCK CERAMICK884889MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.

View all 25 devices →

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑