← Back to catalogue

Panama™

FDA UDI

Class II (US FDA UDI)

by Flospine

Identity

Trade Name
Panama™ FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
Self Tapping Rescue Variable Screw, 4.5x18mm FDA UDI
Model / Reference
Panama™ FDA UDI
Description
Self Tapping Rescue Variable Screw, 4.5x18mm FDA UDI

Identifiers

Catalog Number
08-0245-018 FDA UDI
Primary DI / UDI-DI
B1830802450180 FDA UDI
510(k) Number
K210182 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Spinal fixation plate, non-bioabsorbable

Panama™ by Flospine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Flospine

Sources (1)

  • FDA UDI 5da91e77-7e7a-4b0b-9cb6-06adfd3536f7 36 fields · synced Jun 6, 2026