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Intertan Max 72910928l

by Smith & Nephew, Inc.

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 Number00885556898062 UDI-DI Date10 Nov 2025ListedStatusListed 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  • Withdrawn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
Intertan Max
Generic Name
Femur intramedullary nail
Model / Ref / Catalog
72910928L
Primary DI / UDI-DI
00885556898062
510(k) Number
FDA Product Code
JDS
GMDN Term
Femur intramedullary nail
Device Class
Class II
Regulation Number
888.3030
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Angle — 130 degree
Length — 28 Centimeter

Related devices

Cleared under the same submission (K240061)

Show all (12)

Other devices from Smith & Nephew, Inc.

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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