← Back to catalogue

Pls

FDA UDI

Class II (US FDA UDI)

by Boxspine Holdings, Inc.

Identity

Trade Name
PLS FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Ø5.5 Polyaxial Pedicle Screw Non-Cannulated with Screw Cap Ø6.5 x 35mm (Green) FDA UDI
Model / Reference
06.6380B-K FDA UDI
Description
Ø5.5 Polyaxial Pedicle Screw Non-Cannulated with Screw Cap Ø6.5 x 35mm (Green) FDA UDI

Identifiers

Catalog Number
06.6380B-K FDA UDI
Primary DI / UDI-DI
G463066380BK0 FDA UDI
FDA Product Code
KWP FDA UDI
NKB FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Pls by Boxspine Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

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

Sources (1)

  • FDA UDI 4c61d879-d7bc-4ca4-94d3-fe09cbd5a312 34 fields · synced May 29, 2026