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FDA 510(k)

PMT SUBARACHNOID SCREW, MODEL NO.1350-2

K-Number: K883115 · 1988-08-29

ApplicantPmt Corp.
Decision Date1988-08-29
Product CodeGWM
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PMT SUBARACHNOID SCREW, MODEL NO.1350-2 is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 1988-08-29 under 510(k) number K883115. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT SUBARACHNOID SCREW, MODEL NO.1350-2?

PMT SUBARACHNOID SCREW, MODEL NO.1350-2 is a medical device that received FDA 510(k) clearance on 1988-08-29. The listed applicant is Pmt Corp.. The 510(k) number is K883115.

When did PMT SUBARACHNOID SCREW, MODEL NO.1350-2 receive FDA 510(k) clearance?

PMT SUBARACHNOID SCREW, MODEL NO.1350-2 received FDA 510(k) clearance on 1988-08-29, under 510(k) number K883115.

Who is the listed applicant for PMT SUBARACHNOID SCREW, MODEL NO.1350-2?

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

What is the FDA product code for PMT SUBARACHNOID SCREW, MODEL NO.1350-2?

The FDA product code for PMT SUBARACHNOID SCREW, MODEL NO.1350-2 is GWM.

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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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