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FDA 510(k)

CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO

K-Number: K894959 · 1990-09-14

ApplicantAlphatec Mfg., Inc.
Decision Date1990-09-14
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO is the device name listed in this FDA 510(k) record. The listed applicant is Alphatec Mfg., Inc.. It received FDA 510(k) clearance on 1990-09-14 under 510(k) number K894959. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO?

CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO is a medical device that received FDA 510(k) clearance on 1990-09-14. The listed applicant is Alphatec Mfg., Inc.. The 510(k) number is K894959.

When did CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO receive FDA 510(k) clearance?

CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO received FDA 510(k) clearance on 1990-09-14, under 510(k) number K894959.

Who is the listed applicant for CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO?

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

What is the FDA product code for CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO?

The FDA product code for CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO is JEC.

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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.

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