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FDA 510(k)

MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A

K-Number: K896336 · 1989-12-22

ApplicantMedical Advances, Inc.
Decision Date1989-12-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A is the device name listed in this FDA 510(k) record. The listed applicant is Medical Advances, Inc.. It received FDA 510(k) clearance on 1989-12-22 under 510(k) number K896336. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A?

MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Medical Advances, Inc.. The 510(k) number is K896336.

When did MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A receive FDA 510(k) clearance?

MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A received FDA 510(k) clearance on 1989-12-22, under 510(k) number K896336.

Who is the listed applicant for MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A?

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

What is the FDA product code for MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A?

The FDA product code for MODEL SPINE SURVEYOR-PLUS; CAT. #ACS-10A is LNH.

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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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