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iNSitu Hip System 10-83-0439

by Nextstep Arthropedix

iNSitu Hip System 10-83-0439 is a Class I device made by Nextstep Arthropedix, listed in FDA GUDID since 30 May 2026 (UDI-DI 00810030810391), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810030810391 UDI-DI Date30 May 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
iNSitu Hip System
Generic name
Acetabular orthopaedic reamer
Model / reference
10-83-0439
Primary DI / UDI-DI
00810030810391
FDA product code
HTO
GMDN term
Acetabular orthopaedic reamer
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Nextstep Arthropedix

See all devices from Nextstep Arthropedix →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)