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FDA 510(k)

Altomed Malhotra Platinum Segments

K-Number: K170591 · 2017-06-06

ApplicantAltomed Limited
Decision Date2017-06-06
Product CodeMML
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Altomed Malhotra Platinum Segments is the device name listed in this FDA 510(k) record. The listed applicant is Altomed Limited. It received FDA 510(k) clearance on 2017-06-06 under 510(k) number K170591. The device is classified under product code MML. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Altomed Malhotra Platinum Segments?

Altomed Malhotra Platinum Segments is a medical device that received FDA 510(k) clearance on 2017-06-06. The listed applicant is Altomed Limited. The 510(k) number is K170591.

When did Altomed Malhotra Platinum Segments receive FDA 510(k) clearance?

Altomed Malhotra Platinum Segments received FDA 510(k) clearance on 2017-06-06, under 510(k) number K170591.

Who is the listed applicant for Altomed Malhotra Platinum Segments?

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

What is the FDA product code for Altomed Malhotra Platinum Segments?

The FDA product code for Altomed Malhotra Platinum Segments is MML.

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Related Devices (Code: MML)

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.

K021750LID CHAIN EYELID WEIGHTSJedmed Instrument Co.K011740CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)Meddev Corp.K011115KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010Heinz Kurz GmbH MedizintechnikK003646SUTUREGROOVE WEIGHT SIZING SETIop, Inc.K001123KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111Heinz Kurz GmbH MedizintechnikK994289SUTUREGROOVEIop, Inc.

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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