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Summit Porocoat 1570-11-080

by Depuy Orthopaedics, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295060031 UDI-DI Date24 Mar 2015ListedStatusListed 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  • Withdrawn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
Summit Porocoat
Generic Name
Coated femoral stem prosthesis, one-piece
Model / Ref / Catalog
1570-11-080, 157011080
Primary DI / UDI-DI
10603295060031
FDA Product Code
MRA, LPH, JDI, LZO
GMDN Term
Coated femoral stem prosthesis, one-piece
Device Class
Class III
Regulation Number
888.3358, 888.3350, 888.3353
GUDID distribution status
In Commercial Distribution

Related devices

Category: Coated femoral stem prosthesis, one-piece

Other devices from Depuy Orthopaedics, Inc.

See all devices from Depuy Orthopaedics, Inc. →

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