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Precice® Fast Distractor Max PFD2-000

by Nuvasive Specialized Orthopedics, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00195377039910 UDI-DI Date6 Oct 2020ListedStatusListed 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  • Withdrawn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
Precice® Fast Distractor Max
Generic Name
Orthopaedic surgical procedure kit, non-medicated, single-use
Model / Reference
PFD2-000
Primary DI / UDI-DI
00195377039910
FDA Product Code
HWN
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, single-use
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Orthopaedic surgical procedure kit, non-medicated, single-use

Other devices from Nuvasive Specialized Orthopedics, Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No