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FDA 510(k)

SMOOTH STAPLE IMPLANT

K-Number: K900433 · 1990-11-16

ApplicantInterphase Implants, Inc.
Decision Date1990-11-16
Product CodeMDL
Advisory CommitteeDE
DecisionUnknown

Device Summary

SMOOTH STAPLE IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Interphase Implants, Inc.. It received FDA 510(k) clearance on 1990-11-16 under 510(k) number K900433. The device is classified under product code MDL. It was reviewed by the DE advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SMOOTH STAPLE IMPLANT?

SMOOTH STAPLE IMPLANT is a medical device that received FDA 510(k) clearance on 1990-11-16. The listed applicant is Interphase Implants, Inc.. The 510(k) number is K900433.

When did SMOOTH STAPLE IMPLANT receive FDA 510(k) clearance?

SMOOTH STAPLE IMPLANT received FDA 510(k) clearance on 1990-11-16, under 510(k) number K900433.

Who is the listed applicant for SMOOTH STAPLE IMPLANT?

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

What is the FDA product code for SMOOTH STAPLE IMPLANT?

The FDA product code for SMOOTH STAPLE IMPLANT is MDL.

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Related Devices (Code: MDL)

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.

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Official Source

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

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