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SDS Growing Rod

by Baat Medical Products B.V. 12 variants

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 Number08720629958767 UDI-DI Date30 Mar 2026ListedStatusListed 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  • Withdrawn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

Generic Name
Spinal spring-distraction system spring
Model / Ref / Catalog
SDS Growing Rod, SDS55S100
Primary DI / UDI-DI
08720629958767
510(k) Number
FDA Product Code
PGM
GMDN Term
Spinal spring-distraction system spring
Device Class
Class II
Regulation Number
888.3070
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K251961)

Show all (11)

Other devices from Baat Medical Products B.V.

See all devices from Baat Medical Products B.V. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • 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