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Overwatch

FDA UDI

Class II (US FDA UDI)

by Spinal Elements, Inc.

Identity

Trade Name
OVERWATCH FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
OVERWATCH® 7.5MM x 60MM POLY REDUCTION DUALFIX SCREW FDA UDI
Model / Reference
108-RS-7560D FDA UDI
Description
OVERWATCH® 7.5MM x 60MM POLY REDUCTION DUALFIX SCREW FDA UDI

Identifiers

Primary DI / UDI-DI
00840916137106 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system, non-sterile

Overwatch by Spinal Elements, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spinal Elements, Inc.

Sources (1)

  • FDA UDI 70fe458b-8ca5-40d7-b09b-25f703804c11 33 fields · synced May 31, 2026