FDA.reportPublic FDA data

Overwatch PCF

Primary DI
00840606193412
Brand
Overwatch PCF
Company
SPINAL ELEMENTS, INC.
Model
33073-004
Device description
CT, T15 Screw to Screw Connector, 39-56 mm
Published
2026-07-30
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
NKGPosterior Cervical Screw System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NKGPosterior Cervical Screw SystemOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840606193412PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840606193412008406061934128406061934120840606193412

GMDN Terms#

Term, Definition table
TermDefinition
Bone-screw internal spinal fixation system rodAn implantable component of a bone-screw internal spinal fixation system in the form of a thin cylinder intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. This component is designed as a longitudinal (intervertebral) connecting element passing through the system’s implantable screw heads or hooks. It is available in various forms (e.g., straight, curved, rigid, flexible, with varying diameters); flexible types may allow small movements of the spine.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
7606070121customerservice@spinalelements.com

Regulatory Flags#

DUNS number
610712213
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840606185110LUNA TiLUN20006-10T2026-09-25
00840606185127LUNA TiLUN20006-12T2026-09-25
00840606185134LUNA TiLUN20006-14T2026-09-25
00840606185141LUNA TiLUN20012-12T2026-09-25
00840606185158LUNA TiLUN20012-14T2026-09-25
00840606185165LUNA TiLUN20012-16T2026-09-25
00840606186223ALIF Disc Prep11044-0002026-09-25
00840606186230ALIF Disc Prep15161-0002026-09-25
00840606186261ALIF15163-0022026-09-25
00840606186278ALIF15163-0032026-09-25
00840606186285ALIF15163-0042026-09-25
00840606187381ALIF15301-0002026-09-25
00840606187565Ventana A40050-0202026-09-25
00840606187572Ventana A40050-0252026-09-25
00840606187589Ventana A40050-0302026-09-25
00840606187596Ventana A40050-0352026-09-25
00840606187602Ventana A40060-0202026-09-25
00840606187619Ventana A40060-0252026-09-25
00840606187633Ventana A40060-0352026-09-25
00840606196024Vertu53067-0012026-09-25

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