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FDA 510(k)

TECHMEDICA MP SYSTEM

K-Number: K882922 · 1988-09-22

ApplicantTechmedica, Inc.
Decision Date1988-09-22
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECHMEDICA MP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1988-09-22 under 510(k) number K882922. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHMEDICA MP SYSTEM?

TECHMEDICA MP SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-22. The listed applicant is Techmedica, Inc.. The 510(k) number is K882922.

When did TECHMEDICA MP SYSTEM receive FDA 510(k) clearance?

TECHMEDICA MP SYSTEM received FDA 510(k) clearance on 1988-09-22, under 510(k) number K882922.

Who is the listed applicant for TECHMEDICA MP SYSTEM?

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

What is the FDA product code for TECHMEDICA MP SYSTEM?

The FDA product code for TECHMEDICA MP SYSTEM is KTT.

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Other records listing Techmedica, 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.

K933935CKS POROUS COATED FEMORAL COMPONENTK932017TECHMEDICA CONTINUUM HIP WITH HA COATINGK931929TECHMEDICA CONTINUUM HIP SYSTEMK926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMK925420TECHMEDICA STANDARD BIPOLAR SYSTEMK923808MULLER STRAIGHT STEM FEMORAL PROSTHESIS

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Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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