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SeaSpine Spacer System - Hollywood NanoMetalene 34-5113-S

by SeaSpine Orthopedics Corporation

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 Number00889981034705 UDI-DI Date2 Nov 2016ListedStatusListed 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  • Withdrawn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
SeaSpine Spacer System - Hollywood NanoMetalene
Generic Name
Vertebral body prosthesis
Model / Ref / Catalog
34-5113-S
Primary DI / UDI-DI
00889981034705
FDA Product Code
MAX, MQP
GMDN Term
Vertebral body prosthesis
Device Class
Class II
Regulation Number
888.3080, 888.3060
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vertebral body prosthesis

Cleared under the same submission (K162715)

Show all (12)

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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