FDA.reportPublic FDA data

3P Hip System

Primary DI
00840536800053
Brand
3P Hip System
Company
ORTHOPEDIATRICS CORP.
Model
01-3002-3013
Catalog number
01-3002-3013
Device description
3P Adolescent Beam - Adjustable Cut Guide
Published
2026-06-09
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
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
HRSPlate, fixation, bone

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRSPlate, Fixation, BoneOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K243963000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K243963000Pediatric Plating Platform HipOrthoPediatrics Corp.2025-04-29HRS

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840536800053PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840536800053008405368000538405368000530840536800053

GMDN Terms#

Term, Definition table
TermDefinition
Osteotomy guide, reusableA surgical instrument intended to be attached to a bone (e.g., pelvis, femur, tibia, ulna) during an osteotomy procedure (including during joint arthroplasty) to outline/define the desired cut-line and mechanically support/guide the cutting device (e.g., oscillating cutting saw). This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(574)268-6379xxx@xxx.com

Regulatory Flags#

DUNS number
796416191
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
00841132125014General Instrument01-1003-300101-1003-30012016-09-25
00841132125021General Instrument01-1003-300201-1003-30022016-09-25
00841132125038General Instrument01-1003-300301-1003-30032016-09-25
00841132124277ACL01-1008-253001-1008-25302021-07-06
00841132122112OrthoPediatrics ACL Reconstruction System10-1008-106010-1008-10602015-09-18
00841132122129OrthoPediatrics ACL Reconstruction System10-1008-106510-1008-10652015-09-18
00841132122136OrthoPediatrics ACL Reconstruction System10-1008-107010-1008-10702015-09-18
00841132122143OrthoPediatrics ACL Reconstruction System10-1008-107510-1008-10752015-09-18
00841132122150OrthoPediatrics ACL Reconstruction System10-1008-108010-1008-10802015-09-18
00841132122167OrthoPediatrics ACL Reconstruction System10-1008-108510-1008-10852015-09-18
00841132122174OrthoPediatrics ACL Reconstruction System10-1008-109010-1008-10902015-09-18
00841132122181OrthoPediatrics ACL Reconstruction System10-1008-110010-1008-11002015-09-18
00841132122198OrthoPediatrics ACL Reconstruction System10-1008-406010-1008-40602015-09-18
00841132122204OrthoPediatrics ACL Reconstruction System10-1008-406510-1008-40652015-09-18
00841132122211OrthoPediatrics ACL Reconstruction System10-1008-407010-1008-40702015-09-18
00841132122228OrthoPediatrics ACL Reconstruction System10-1008-407510-1008-40752015-09-18
00841132122235OrthoPediatrics ACL Reconstruction System10-1008-408010-1008-40802015-09-18
00841132122242OrthoPediatrics ACL Reconstruction System10-1008-408510-1008-40852015-09-18
00841132126219General Instrument01-1008-000701-1008-00072016-09-25
00841132126226General Instrument01-1008-001001-1008-00102016-09-25

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