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510(k) K170591

Altomed Malhotra Platinum Segments by Altomed Limited — Product Code MML

K170591 is an FDA 510(k) premarket notification submitted by Altomed Limited for the device "Altomed Malhotra Platinum Segments". The FDA issued a decision of Substantially Equivalent on June 6, 2017. The device falls under product code MML (Weights, Eyelid, External), a Class II device regulated under 21 CFR 886.5700.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 2017
Date Received
February 28, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Weights, Eyelid, External
Device Class
Class II
Regulation Number
886.5700
Review Panel
OP
Submission Type

Gravity assisted treatment of lagophthalmos (incomplete eyelid closure)

Other clearances for product code MML

  • K150986 — Contour Eyelid Weight Implants, ThinProfile Eyelid Weight Implants (August 17, 2015)
  • K021750 — LID CHAIN EYELID WEIGHTS (January 27, 2003)
  • K011740 — CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000) (July 2, 2001)
  • K011115 — KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL (May 2, 2001)
  • K003646 — SUTUREGROOVE WEIGHT SIZING SET (February 22, 2001)
  • K001123 — KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111 (April 21, 2000)
  • K994289 — SUTUREGROOVE (April 17, 2000)
  • K000127 — KURZ PURE GOLD UPPER EYELIDS IMPLANT (OBERASCHER), MODEL 4001 02-4001 10 (April 12, 2000)
  • K990224 — LABTICIAN LID LOAD EXTERNAL EYELID SIZING SET (April 12, 1999)
  • K983607 — LABTICIAN LID LOAD GOLD EYELID WEIGHT IMPLANTS (January 8, 1999)

FDA data resources