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MOTO Partial Knee System - Medial 02.18.IF7.10.LM

by Medacta International

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07630030896491 UDI-DI Date9 Jan 2017ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
MOTO Partial Knee System - Medial
Generic Name
Unicondylar knee insert
Model / Reference
02.18.IF7.10.LM
Primary DI / UDI-DI
07630030896491
510(k) Number
FDA Product Code
HSX
GMDN Term
Unicondylar knee insert
Device Class
Class II
Regulation Number
888.3520
GUDID distribution status
In Commercial Distribution

Related devices

Category: Unicondylar knee insert

Cleared under the same submission (K162084)

Show all (12)

Other devices from Medacta International

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No