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Pedicle Marker With Head 98371-1000

by Captiva Spine

Pedicle Marker With Head 98371-1000 is a Class I device made by Captiva Spine, listed in FDA GUDID since 23 Oct 2026 (UDI-DI M739983711000), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM739983711000 UDI-DI Date23 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pedicle Marker With Head
Generic name
General internal orthopaedic fixation system implantation kit
Model / reference
98371-1000
Primary DI / UDI-DI
M739983711000
FDA product code
KIL
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

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